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        <title>MedWorm: Chemistry</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 5000 RSS medical sources are combined and output via different filters. This feed contains the latest headlines from journals and sites in the Chemistry category.</description>
        <link><![CDATA[http://www.medworm.com/rss/index.php/Chemistry/59/]]></link>
        <lastBuildDate>Sun, 06 Jul 2008 10:19:49 +0100</lastBuildDate>
        <comments>http://www.medworm.com/rss/comments.php?id=</comments>
        <item>
            <title>Xvi-sibee: the xvi brazilian symposium of electrochemistry and electroanalytical chemistry</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0103-50532008000400001&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description> (Source: Journal of the Brazilian Chemical Society) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Journal of the Brazilian Chemical Society</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581322</comments>
            <pubDate>Sat, 05 Jul 2008 15:35:21 +0100</pubDate>
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            <title>Experimental study of fluidized bed agglomeration of acerola powder</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0104-66322008000100007&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description>The aim of this work was to study the main effects of acerola powder on fluidized bed agglomeration. A 2(4-1) fractional factoring design was used to evaluate the main operating conditions (fluidizing air temperature, fluidizing air velocity, atomizing air flow and height of nozzle in the bed). The mechanical and physicochemical product changes were determined by analysis of particle diameter, moisture content, wetting time and bed porosity. The particle enlargement by agglomeration occurred when the relative humidity in the bed increased and, thus, the moisture of the product increased. However, the excessive increase in relative humidity resulted in a decrease in yield, caused by caking and product incrustation. The consolidation of small granules resulted in an increase in the instant properties, decreasing the wetting time and increasing the solubility in a short period of agitation. (Source: Brazilian Journal of Chemical Engineering) </description>
            <author>Brazilian Journal of Chemical Engineering</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581293</comments>
            <pubDate>Sat, 05 Jul 2008 15:34:48 +0100</pubDate>
            <guid isPermaLink="false">1581293</guid>        </item>
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            <title>Simultaneous heat and mass transfer in packed bed brying of seeds having a mucilage coating</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0104-66322008000100006&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description>The simultaneous heat and mass transfer between fluid phase and seeds having a mucilaginous coating was studied during packed bed drying. To describe the process, a two-phase model approach was employed, in which the effects of bed shrinkage and nonconstant physical properties were considered. The model took into account bed contraction by employing moving coordinates. Equations relating shrinkage and structural parameters of the packed bed with moisture content, required in the drying model, were developed from experimental results in thick-layer bed drying. The model verification was based on a comparison between experimental and predicted data on moisture content and temperature along the bed. Parametric studies showed that the application of correlations capable of incorporating changes in bed properties gives better data simulation. By experimental-theoretical analysis, the importance of shrinkage for a more accurate interpretation of heat and mass transfer phenomena in the drying of porous media composed of mucilaginous seeds is corroborated. (Source: Brazilian Journal of Chemical Engineering) </description>
            <author>Brazilian Journal of Chemical Engineering</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581292</comments>
            <pubDate>Sat, 05 Jul 2008 15:34:48 +0100</pubDate>
            <guid isPermaLink="false">1581292</guid>        </item>
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            <title>Characteristics of flow in wet conical spouted beds of unequal-sized spherical particles</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0104-66322008000100005&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description>Interparticle forces, developed in wet spouted beds composed of a mixture of spherical particles with different size distributions, intensify particle segregation mechanisms interfering in gas distribution inside the bed and, consequently, in the spouting flow characteristics. Therefore, this paper is aimed at describing the effect of interparticle forces on the air-solid flow distribution in conical spouted beds of unequal-sized particles coated by a thin glycerol film. Experimental results show that both the minimum spouting airflow rate and the minimum spouting pressure drop decrease as the amount of glycerol added to the bed increases. In addition, simulated results of the annular air velocity along the bed height showed that, at the base of the column, the radial component of the inertial force is high enough to break liquid bridges between particles and carry these particles out along the spout. Moreover, as the glycerol concentration increases, the spout diameter increases along the bed height. Such changes in the air-solid flow can maintain the spouting regime for higher glycerol concentrations as shown by experimental data. (Source: Brazilian Journal of Chemical Engineering) </description>
            <author>Brazilian Journal of Chemical Engineering</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581291</comments>
            <pubDate>Sat, 05 Jul 2008 15:34:48 +0100</pubDate>
            <guid isPermaLink="false">1581291</guid>        </item>
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            <title>Mass transfer inside oblate spheroidal solids: modelling and simulation</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0104-66322008000100004&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description>A numerical solution of the unsteady diffusion equation describing mass transfer inside oblate spheroids, considering a constant diffusion coefficient and the convective boundary condition, is presented. The diffusion equation written in the oblate spheroidal coordinate system was used for a two-dimensional case. The finite-volume method was employed to discretize the basic equation. The linear equation set was solved iteratively using the Gauss-Seidel method. As applications, the effects of the Fourier number, the Biot number and the aspect ratio of the body on the drying rate and moisture content during the process are presented. To validate the methodology, results obtained in this work are compared with analytical results of the moisture content encountered in the literature and good agreement was obtained. The results show that the model is consistent and it may be used to solve cases such as those that include disks and spheres and/or those with variable properties with small modifications. (Source: Brazilian Journal of Chemical Engineering) </description>
            <author>Brazilian Journal of Chemical Engineering</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581290</comments>
            <pubDate>Sat, 05 Jul 2008 15:34:48 +0100</pubDate>
            <guid isPermaLink="false">1581290</guid>        </item>
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            <title>Modelling and automation of the process of phosphate ion removal from waste waters</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0104-66322008000100003&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description>Phosphate removal from waste waters has become an environmental necessity, since these phosphates stimulate the growth of aquatic plants and planktons and contribute to the eutrophication process in general. The physicochemical methods of phosphate ion removal are the most effective and reliable. This paper presents studies on the process of phosphate ion removal from waste waters resulting from the fertiliser industrys use of the method of co-precipitation with iron salts and with calcium hydroxide as the neutralizing agent. The optimal process conditions were established as those that allow achievement of a maximum degree of separation of the phosphate ions. The precipitate resulting from the co-precipitation process was analysed for chemical composition and establishment of thermal and structural stability, and the aim was also to establish in which form the phosphate ions in the formed precipitate can be found. Based on these considerations, the experimental data obtained in the process of phosphate ion removal from waste waters were analysed mathematically and the equations for the dependence of the degree of phosphate separation and residual concentration versus the main parameters of the process were formulated. In this paper an automated scheme for the phosphate ion removal from waste waters by co-precipitation is presented. (Source: Brazilian Journal of Chemical Engineering) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Brazilian Journal of Chemical Engineering</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581289</comments>
            <pubDate>Sat, 05 Jul 2008 15:34:48 +0100</pubDate>
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            <title>Production of enantiomerically pure d-phenylglycine using pseudomonas aeruginosa 10145 as biocatalyst</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0104-66322008000100002&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description>Different bacterial strains were screened to detect nitrilase and/or nitrile hidratase/amidase activities towards benzonitrile, to be used as biocatalyst to produce enantiomerically pure non-proteinogenic amino acids using amino nitriles as starting material. The best biocatalyst found was Pseudomonas aeruginosa 10145, which showed high enzyme activities. Whole cells were used as catalyst for the transformation of 2-phenyl-2-amino-acetonitrile for the corresponding D-phenylglycine. The percentage conversion was followed by chiral HPLC. After 1 hour reaction 18% of 2-phenyl-2-amino-acetonitrile was converted into D-phenylglycine with an enantiomeric excess of over 95%. When an inducer was added to the media, an increase in nitrile hydrolyzing activities was detected, hence leading to total conversion of (R)-2-phenyl-2-amino-acetonitrile to the corresponding amino acid in 30 min reaction. The isolated yield of the target product was 50% and its characterization was performed by polarimetry, chiral HPLC, IR-FT spectroscopy and GC-MS. (Source: Brazilian Journal of Chemical Engineering) </description>
            <author>Brazilian Journal of Chemical Engineering</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581288</comments>
            <pubDate>Sat, 05 Jul 2008 15:34:48 +0100</pubDate>
            <guid isPermaLink="false">1581288</guid>        </item>
        <item>
            <title>Editorial: announcement</title>
            <link>http://www.scielo.br/scielo.php?script=sci_arttext&amp;pid=S0104-66322008000100001&amp;lng=en&amp;nrm=iso&amp;tlng=en</link>
            <description> (Source: Brazilian Journal of Chemical Engineering) </description>
            <author>Brazilian Journal of Chemical Engineering</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1581287</comments>
            <pubDate>Sat, 05 Jul 2008 15:34:48 +0100</pubDate>
            <guid isPermaLink="false">1581287</guid>        </item>
        <item>
            <title>Lithium manganese(ii) diaquaborophosphate monohydrate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?mg2052</link>
            <description>The title compound, LiMn(H2O)2[BP2O8]·H2O, is built up of an open framework of helical borophosphate ribbons interconnected by MnO4(H2O)2 octahedra, forming one-dimensional channels along [001] occupied by Li+ cations and disordered H2O molecules (site occupancy 0.5). The Li cations reside in two partially occupied sites [occupancies = 0.42 (3) and 0.289 (13)] near the helices. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578251</comments>
            <pubDate>Sat, 05 Jul 2008 13:15:59 +0100</pubDate>
            <guid isPermaLink="false">1578251</guid>        </item>
        <item>
            <title>A new spin on sorting nanotubes</title>
            <link>http://www.rsc.org/chemistryworld/News/2008/July/03070801.asp</link>
            <description>A technique that separates semiconducting and metallic nanotubes could pave the way for progress in nanoelectronics (Source: Chemistry World | Latest News) </description>
            <author>Chemistry World | Latest News</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1576403</comments>
            <pubDate>Sat, 05 Jul 2008 06:21:44 +0100</pubDate>
            <guid isPermaLink="false">1576403</guid>        </item>
        <item>
            <title>Creating a second genetic code</title>
            <link>http://www.rsc.org/chemistryworld/News/2008/July/04070801.asp</link>
            <description>Scientists have created artificial DNA strands that could form a new biological data storage system (Source: Chemistry World | Latest News) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Chemistry World | Latest News</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1576402</comments>
            <pubDate>Sat, 05 Jul 2008 06:21:44 +0100</pubDate>
            <guid isPermaLink="false">1576402</guid>        </item>
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            <title>Diethyl [2,2,2-trifluoro-1-phenylsulfonylamino-1-(trifluoromethyl)ethyl]phosphonate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?si2094</link>
            <description>The title compound, C13H16F6NO5PS, is of interest with respect to inhibition of serine hydrolases. Its structure contains a 1.8797 (13) Å P—C bond and two intermolecular N—H...O=P hydrogen bonds, resulting in centrosymmetric dimers. An intramolecular N—H...O=P hydrogen bond is also present. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578321</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578321</guid>        </item>
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            <title>(3r,3as,6ar)-2,5-dimethyl-3-(5-phenyl-2-thienyl)perhydropyrrolo[3,4-d][1,2]oxazole-4,6-dione</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?hk2484</link>
            <description>The crystal structure of the title compound, C17H16N2O3S, exhibits intramolecular C—H...S and intermolecular C—H...S and C—H...O hydrogen bonds, C—S...N [S...N = 3.033 (2) Å and C—S...N = 142.76 (9)°] interactions, and C—H...π interactions; these interactions generate S(4), S(6) and R22(14) ring motifs. The isoxazole ring adopts an envelope conformation, with the N atom displaced by 0.672 (2) Å from the plane of the other ring atoms. The thiophene ring is oriented with respect to the succinimide and phenyl rings at dihedral angles of 40.03 (12) and 5.21 (13)°, respectively. The dihedral angle between the succinimide and phenyl rings is 39.38 (12)°. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578320</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578320</guid>        </item>
        <item>
            <title>N-(2-hydroxyethyl)-3,5-dinitrobenzamide</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?lx2057</link>
            <description>The title compound, C9H9N3O6, was synthesized by the condensation of methyl 3,5-dinitrobenzoate and 2-aminoethanol. The non-centrosymmetric space group results in the formation of pseudo-chiral helices in the crystal structure, which exhibits a layer packing structure involving intramolecular N—H...O and O—H...O interactions. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578319</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578319</guid>        </item>
        <item>
            <title>N-(2-chlorophenyl)-2-methylbenzamide</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?bg2196</link>
            <description>In the structure of the title compound (N2CP2MBA), C14H12ClNO, the conformations of the N—H and C=O bonds are trans to each other. Furthermore, the conformation of the N—H bond is syn to the ortho-chloro group in the aniline ring and the C=O bond is syn to the ortho-methyl substituent in the benzoyl ring, similar to what is observed in 2-chloro-N-(2-chlorophenyl)benzamide and 2-methyl-N-phenylbenzamide. The amide group makes almost the same dihedral angles of 41.2 (14) and 42.2 (13)° with the aniline and benzoyl rings, respectively, while the dihedral angle between the benzoyl and aniline rings is only 7.4 (3)°. The molecules in N2CP2MBA are packed into chains through N—H...O hydrogen bonds. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578318</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578318</guid>        </item>
        <item>
            <title>6β-chloro-5α-hydroxy-20-oxopregnan-3β-yl acetate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?im2073</link>
            <description>The title steroid, C23H35ClO4, is a pregnane derivative prepared by ring opening of the corresponding 5α,6α-epoxy steroid with BiCl3. There are two symmetry-independent molecules in the asymmetric unit that show no significant differences concerning bond lengths and angles. The conformation of the six-membered rings in both molecules is close to a chair form, while the five-membered ring adopts an envelope conformation. All rings in both molecules are trans-fused. The molecules are held together by an extensive O—H...O hydrogen-bonding network. (Source: Acta Crystallographica Section E) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578317</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578317</guid>        </item>
        <item>
            <title>2-[3,4-dibutoxy-5-(5-phenyl-1,3,4-oxadiazol-2-yl)-2-thienyl]-5-phenyl-1,3,4-oxadiazole</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?hb2756</link>
            <description>In the title compound, C28H28N4O4S, the dihedral angles between the central thiophene ring and its pendant oxadiazole rings are 1.2 (3) and 9.8 (3)°. The dihedral angles between the oxadiazole and phenyl rings are 2.9 (3) and 1.8 (3)°. Some short intramolecular C—H...O contacts occur. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578316</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578316</guid>        </item>
        <item>
            <title>(e)-6-methoxy-9-methyl-1,2,3,4-tetrahydro-9h-carbazol-4-one oxime</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?om2245</link>
            <description>The title compound, C14H16N2O2, is dimerized by inversion-related intermolecular O—H...O and O—H...N hydrogen bonding. There is also an intramolecular C—H...N bond, resulting in a six-membered ring. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578315</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578315</guid>        </item>
        <item>
            <title>Methyl 6-bromo-7-methoxy-1,3-benzodioxole-5-carboxylate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?tk2272</link>
            <description>The non-H atoms of the title compound, C10H9BrO5, are essentially coplanar, with the exception of the ester group [the O=C—O—C torsion angle is −143.4 (3)°]. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578314</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578314</guid>        </item>
        <item>
            <title>1,4-diazoniabicyclo[2.2.2]octane bis(2-chlorobenzoate)</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?bx2155</link>
            <description>The title compound, C6H14N22+·2C7H4ClO2−, contains trimeric units linked by N—H...O hydrogen bonds. The carboxylate groups of the 2-chlorobenzoate anions form dihedral angles of 66.1 (1) and 76.1 (1)° with the respective chlorobenzene rings to which they are bound. The hydrogen-bonded trimers are arranged in layers in the (200) planes and the chlorobenzoate anions form edge-to-face interactions between layers, with dihedral angles of 61.9 (1) and 49.8 (1)° and centroid–centroid distances of 4.85 (1) and 4.65 (1) Å, respectively, for two crystallographically distinct interactions. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578313</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578313</guid>        </item>
        <item>
            <title>6-bromo-3-hydroxy-4-oxo-2-phenyl-4h-chromene-8-carboxylic acid dimethylformamide disolvate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?dn2358</link>
            <description>In the title compound, C16H9BrO5·2C3H7NO, the chromene ring system is essentially planar. The two dimethylformamide solvent molecules are linked by intermolecular O—H...O hydrogen bonds to the 6-bromo-3-hydroxy-4-oxo-2-phenyl-4H-chromene-8-carboxylic acid molecules. (Source: Acta Crystallographica Section E) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578312</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578312</guid>        </item>
        <item>
            <title>1-(2-furoyl)-3-(o-tolyl)thiourea</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?ci2623</link>
            <description>The title compound, C13H12N2O2S, was synthesized from furoyl isothiocyanate and o-toluidine in dry acetone. The thiourea group is in the thioamide form. The central thiourea fragment makes dihedral angles of 2.6 (1) and 22.4 (1)° with the ketofuran group and the benzene ring, respectively. The molecular structure is stabilized by N—H...O hydrogen bonds. In the crystal structure, centrosymmetrically related molecules are linked by a pair of N—H...S hydrogen bonds to form a dimer with an R22(6) ring motif. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578311</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578311</guid>        </item>
        <item>
            <title>(1e,4e)-1,5-bis(4-methylphenyl)penta-1,4-dien-3-one</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?bq2087</link>
            <description>The title compound, C19H18O, crystallizes in a non-centrosymmetric space group although the molecule has no chiral centre. The dihedral angle between the aromatic rings is 20.43 (13)°. The structure is stabilized by two intramolecular hydrogen bonds, and by four π–π and three C—H...π interactions between the aromatic rings. The perpendicular distances between the centroids of the rings involved in the π–π interactions have values of 1.996, 2.061, 2.181 and 2.189 Å. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578310</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578310</guid>        </item>
        <item>
            <title>2-[(e)-(5-amino-2,3-diphenylquinoxalin-6-yl)iminomethyl]-4-chlorophenol</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?tk2279</link>
            <description>The title Schiff base compound, C27H19ClN4O, features two intramolecular O—H...N and N—H...N hydrogen bonds involving the hydroxy and amino groups to generate S(6) and S(5) ring motifs, respectively. In the crystal structure, weak intermolecular N—H...O and C—H...N interactions, together with π–π contacts [centroid–centroid distances = 3.6294 (11)–3.6881 (11) Å], link neighboring molecules. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578309</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578309</guid>        </item>
        <item>
            <title>2,2,2-trimethyl-n-(phenylsulfonyl)acetamide</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?rz2222</link>
            <description>The N—H and C=O bonds of the SO2—NH—CO group in the title compound, C11H15NO3S, are anti to each other. The asymmetric unit contains two independent molecules. The benzene rings form dihedral angles of 83.19 (8) and 76.01 (10)° with the mean planes of the C2NOS fragments. The molecules are linked into chains parallel to the b axis by intermolecular N—H...O hydrogen bonds. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578308</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578308</guid>        </item>
        <item>
            <title>Methyl 2-(7-benzyloxy-1-naphthyl)-2-oxoacetate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?is2310</link>
            <description>In the crystal structure of the title compound, C20H16O4, the naphthalene ring system makes dihedral angles of 43.79 (7) and 83.70 (9)°, respectively, with the mean planes of the phenyl ring and the acetate unit. C—H...π interactions involving all the aromatic six-membered rings are observed. The molecules are stacked into columns along the a axis and adjacent columns are linked by weak C—H...O interactions. (Source: Acta Crystallographica Section E) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578307</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578307</guid>        </item>
        <item>
            <title>Di-tert-butyl 2,2′-(biphenyl-2,2′-diyldioxy)diacetate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?ez2127</link>
            <description>The title compound, C24H30O6, does not exhibit π–π interactions due to the steric effect of the bulky tert-butyl groups present in the molecule. The presence of these groups at the 2 and 2′ positions hinders the free motion of the benzene rings relative to each other, causing them to adopt an antiperiplanar arrangement. The benzene rings are twisted by just under 50.96 (17)° with respect to each other. The carbonyl groups within the molecule are directed in different directions, one towards the biphenyl group and the other away from it. The molecules are linked together by C=O...H—C hydrogen bonds. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578306</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578306</guid>        </item>
        <item>
            <title>N-(2-chlorobenzoyl)-n′-(3-pyridyl)thiourea</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?rz2227</link>
            <description>In the molecule of the title compound, C13H10ClN3OS, the dihedral angles between the plane through the thiourea group and the pyridine and benzene rings are 53.08 (3) and 87.12 (3)°, respectively. The molecules are linked by intermolecular N—H...N hydrogen-bonding interactions to form a supramolecular chain structure along the a axis. An intramolecular N—H...O hydrogen bond is also present. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578305</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578305</guid>        </item>
        <item>
            <title>2-(4-methoxyphenyl)-1h-indene</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?wk2085</link>
            <description>Excluding four H atoms, the molecule of the title compound, C16H14O, is almost planar, with an r.m.s. deviation of 0.0801 (2) Å. Due to p–π conjugation, the lengths of the two single bonds attached to the O atom are significantly different. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578304</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578304</guid>        </item>
        <item>
            <title>1,1′-[(hexane-1,6-diyldioxy)bis(nitrilomethylidyne)]dinaphthalene</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?hg2416</link>
            <description>The title compound, C28H28N2O2, was synthesized by condensation of 1-naphthaldehyde with 1,6-bis(aminooxy)hexane in ethanol. The molecule is disposed about a crystallographic centre of symmetry. In the crystal structure, molecules are linked through strong intermolecular π–π stacking interactions [interplana distance = 2.986 (2) Å], forming a three-dimensional network. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578303</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578303</guid>        </item>
        <item>
            <title>N-[(5-chloro-3-methyl-1-phenyl-1h-pyrazol-4-yl)carbonyl]-n′-(4-hydroxyphenyl)thiourea</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?gk2153</link>
            <description>In the title compound, C18H15ClN4O2S, the pyrazole ring makes dihedral angles of 67.4 (1) and 12.5 (1)° with the phenyl and 4-hydroxyphenyl groups, respectively; the two benzene rings are twisted by 60.1 (1)° with respect to each other. The thiourea NH groups are involved in N—H...O and N—H...Cl intramolecular hydrogen bonds. A hydrogen bond between the phenolic OH group and the pyrazole N atom connects molecules into a one-dimensional polymeric structure. (Source: Acta Crystallographica Section E) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578302</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578302</guid>        </item>
        <item>
            <title>5-(1h-1,2,3-benzotriazol-1-ylmethyl)-3-phenyl-1,2,4-oxadiazole</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?lh2650</link>
            <description>In the title molecule, C15H11N5O, the 1,2,3-benzotriazole and 3-phenyl-1,2,4-oxadiazole units are individually essentially planar and the dihedral angle between them is 80.2 (2)°. In the crystal structure, molecules are connected via weak intermolecular C—H...N hydrogen bonds to form two-dimensional sheets. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578301</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578301</guid>        </item>
        <item>
            <title>6-(3-pyridyl)-3-(3,4,5-trimethoxyphenyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?hk2481</link>
            <description>In the molecule of the title compound, C17H15N5O3S, the planar central heterocylic ring system is oriented with respect to the benzene and pyridine rings at dihedral angles of 6.61 (3) and 19.22 (3)°, respectively. An intramolecular C—H...N hydrogen bond results in the formation of a six-membered ring, adopting a flattened boat conformation. In the crystal structure, intermolecular C—H...N hydrogen bonds link the molecules. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578300</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578300</guid>        </item>
        <item>
            <title>4-methoxyphenyl 2,3,4,6-tetra-o-acetyl-1-thio-α-d-mannopyranoside</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?lh2646</link>
            <description>The title compound, C21H26O10S, was synthesized in a single step from mannose pentaacetate. The molecular structure confirms the α configuration of the anomeric thioaryl substituent. Spectroscopic and melting-point data obtained for the title compound are in disagreement with those previously reported, indicating the previously reported synthesis [Durette &amp; Shen (1980). Carbohydr. Res. 81, 261–274] to be erroneous. The crystal structure is stabilized by weak intermolecular C—H...O hydrogen bonds. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578299</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578299</guid>        </item>
        <item>
            <title>3-ethyl-4-[(e)-2-methylbenzylideneamino]-1h-1,2,4-triazole-5(4h)-thione</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?xu2434</link>
            <description>Crystals of the title compound, C12H14N4S, were obtained from a condensation reaction of 4-amino-3-ethyl-1H-1,2,4-triazole-5(4H)-thione and 2-methylbenzaldehyde. In the molecular structure, there is a short N=C double bond [1.255 (2) Å], and the benzene and triazole rings are located on opposite sites of this double bond. The two rings are approximately parallel to each other, the dihedral angle being 1.75 (11)°. A partially overlapped arrangement is observed between the nearly parallel triazole and benzene rings of adjacent molecules; the perpendicular distance of the centroid of the triazole ring from the benzene ring is 3.482 Å, indicating the existence of π–π stacking in the crystal structure. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578298</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578298</guid>        </item>
        <item>
            <title>4-(2-benzoylethyl)benzoic acid</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?fl2203</link>
            <description>The title compound, C16H14O3, adopts a conformation in which each functional group is almost coplanar with its adjacent ring, while the two aromatic rings are twisted with respect to one another with a dihedral angle of 78.51 (3)°. The compound dimerizes by standard centrosymmetric hydrogen-bonded carboxyl pairing [O...O = 2.6218 (11) Å and O—H...O = 176 (2)°]. The packing includes two intermolecular C—H...O close contacts with the ketone group. (Source: Acta Crystallographica Section E) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578297</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578297</guid>        </item>
        <item>
            <title>(e)-2-(benzyliminomethyl)-4,6-dibromophenol</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?lx2061</link>
            <description>The title compound, C14H11Br2NO, was prepared by the condensation of benzylamine and 3,5-dibromo-2-hydroxybenzaldehyde. The crystal structure is stabilized by aromatic π–π stacking interactions between the phenol rings of neighbouring molecules [centroid–centroid distance = 3.530 (5) Å]. In addition, the stacked molecules exhibit intermolecular C—H...π and intramolecular O—H...N interactions. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578296</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578296</guid>        </item>
        <item>
            <title>Methyl n′-[(e)-4-hydroxy-3-methoxybenzylidene]hydrazinecarboxylate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?hb2754</link>
            <description>The molecule of the title compound, C10H12N2O4, adopts a trans configuration with respect to the C=N double bond. The dihedral angle between the benzene ring and the hydrazinecarboxylate mean plane is 36.54 (6)°. The molecules are linked into a two-dimensional network by intermolecular O—H...O, N—H...O and O—H...N hydrogen bonds, and by aromatic π–π stacking interactions [ring-centroid separation 3.7689 (9) Å]. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578295</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578295</guid>        </item>
        <item>
            <title>Ethyl n′-[(e)-4-hydroxybenzylidene]hydrazinecarboxylate at 123 k</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?ci2620</link>
            <description>The molecule of the title compound, C10H12N2O3, adopts a trans configuration with respect to the C=N bond. The dihedral angle between the benzene ring and the hydrazinecarboxylate plane is 14.6 (1)°. Molecules are linked into a three-dimensional network by O—H...O, N—H...O and C—H...O hydrogen bonds, and by C—H...π interactions. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578294</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578294</guid>        </item>
        <item>
            <title>2,5,7-trimethyl-3-phenylsulfinyl-1-benzofuran</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?rn2045</link>
            <description>The title compound, C17H16O2S, was prepared by the oxidation of 2,5,7-trimethyl-3-phenylsulfanyl-1-benzofuran with 3-chloroperoxybenzoic acid. The O atom and the phenyl group of the phenylsulfinyl substituent lie on opposite sides of the plane of the benzofuran fragment. The phenyl ring is nearly perpendicular to the plane of the benzofuran unit [88.30 (9)°] and is tilted slightly towards it. No π–π or C—H...π interactions are observed between neighbouring molecules in the crystal structure because of steric hindrance induced by the three methyl groups. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578293</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578293</guid>        </item>
        <item>
            <title>(1α,2β,3α,7α,11α,13β)-1,3,11-triacetoxy-2,13-bis(benzyloxy)-7-hydroxy-21-methyl-n,19-secohetisan-19-al</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?xu2424</link>
            <description>The title compound (delgradine), C41H43NO12, is a hetisine-type C20-diterpenoid alkaloid, isolated from the roots of Aconitum carmichaeli Debx. In the crystal structure, the molecule assumes an U-shaped conformation, the terminal benzene rings being approximately parallel and partially overlapped with each other. The molecule contains eight alicyclic and heterocyclic rings. Cyclohexane rings A and B adopt similar chair conformations; the six-membered rings C, D and E form a bicyclo[2.2.2]octane system with a boat conformation for each six-membered ring, the six-membered heterocyclic ring F has a screw-boat conformation and both of the five-membered rings G and H have envelope conformations. The crystal structure contains intermolecular O—H...O hydrogen bonding. (Source: Acta Crystallographica Section E) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578292</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578292</guid>        </item>
        <item>
            <title>N-phenyladamantane-1-sulfinamide</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?lx2059</link>
            <description>In the racemic title compound, C16H21NOS, the molecules are packed into polymeric chains in the b-axis direction and are linked along the b axis by N—H...O and C—H...O hydrogen bonds. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578291</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578291</guid>        </item>
        <item>
            <title>Methyl 2-acetonyl-4-hydroxy-2h-1,2-benzothiazine-3-carboxylate 1,1-dioxide</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?bt2729</link>
            <description>In the molecule of the title compound, C13H13NO6S, the thiazine ring adopts a distorted sofa conformation. The enolic H atom is involved in intramolecular O—H...O hydrogen bonding besides the weaker C—H...O=S and C—H...O=C interactions. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578290</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578290</guid>        </item>
        <item>
            <title>1-acetyl-3-(4-chlorophenyl)-5-(4-fluorophenyl)-2-pyrazoline</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?at2570</link>
            <description>In the title molecule, C17H14ClFN2O, the mean plane of the pyrazoline ring makes dihedral angles of 18.19 (1) and 83.51 (4)° with the 4-chlorobenzene and 4-fluorobenzene rings, respectively. The two benzene rings make a dihedral angle of 76.11 (2)°. Weak intermolecular C—H...O hydrogen bonds help stabilize the crystal structure. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578289</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578289</guid>        </item>
        <item>
            <title>3-chlorophenyl 4-methylbenzoate</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?hk2479</link>
            <description>The crystal structure of the title compound 3CP4MBA, C14H11ClO2, resembles those of 3-methylphenyl 4-methylbenzoate (3MP4MBA), 4-methylphenyl 4-methylbenzoate (4MP4MBA), 4-methylphenyl 4-chlorobenzoate (4CP4MBA) and other aryl benzoates with similar bond parameters. The dihedral angle between the benzene rings in 3CP4MBA is 71.75 (7)°, compared with 56.82 (7)° in 3MP4MBA and 63.57 (5)° in 4MP4MBA. In the crystal structure, the molecules are aligned with their long axis approximately along the [101] direction and stacked along the c axis. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578288</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578288</guid>        </item>
        <item>
            <title>N-(4-bromophenylsulfonyl)-2,2,2-trimethylacetamide</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?bx2154</link>
            <description>The conformations of the N—H and C=O bonds in the SO2—NH—CO—C group of the title compound (N4BPSTMAA), C11H14BrNO3S, are trans to each other, similar to what is observed in N-(4-chlorophenylsulfonyl)-2,2,2-trimethylacetamide (N4CPSTMAA) and 2,2,2-trimethyl-N-(4-methylphenylsulfonyl)acetamide (N4MPSTMAA). The bond parameters in N4BPSTMAA are similar to those in N4CPSTMAA, N4MPSTMAA, N-aryl-2,2,2-trimethylacetamides and 4-bromobenzenesulfonamide. The benzene ring and the SO2—NH—CO—C group in N4BPSTMAA form a dihedral angle of 82.8 (1)°, comparable with the values of 82.2 (1)° in N4CPSTMAA and 71.2 (1)° in N4MPSTMAA. N—H...O hydrogen bonds form a centrosymmetric ring characterized by an R22(8) motif. (Source: Acta Crystallographica Section E) &lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Sponsored Message:&lt;/i&gt;&lt;/b&gt; Find out how you can &lt;a href=&quot;http://www.medworm.com/rss/medicalsponsorship.php&quot; target=&quot;_self&quot;&gt;get your message across here&lt;/a&gt; by sponsoring this MedWorm news feed.&lt;/p&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578287</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578287</guid>        </item>
        <item>
            <title>4-n-butyl-3-(3-methylphenyl)-1h-1,2,4-triazol-5(4h)-one</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?bt2734</link>
            <description>In the molecule of the title compound, C13H17N3O, the two rings make a dihedral angle of 56.63 (13)°. Molecules are linked by strong N—H...O intermolecular hydrogen bonds into chains running along the c axis. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578286</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1578286</guid>        </item>
        <item>
            <title>2-iodo-n-(2-nitrophenylsulfanyl)aniline</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?fl2204</link>
            <description>In title compound, C12H9IN2O2S, the nitro group is rotated slightly, by 8.91 (3)°, out of the plane of the aromatic ring to which it is bonded. Between the two aromatic rings the CSN plane is at a dihedral angle of 84.0 (7)° to the HNC plane. Molecules are linked by C—H...O interactions into a double helical supramolecular architecture. There are no iodo–nitro, π–π or C—H...π(arene) interactions. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578285</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
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            <title>2-methylbenzaldehyde 2-methylbenzylidenehydrazone</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?hb2750</link>
            <description>The molecule of the title compound, C16H16N2, is centrosymmetric and the dihedral angle between the benzene ring and the dimethylhydrazine mean plane is 16.11 (15)°. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578284</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
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        <item>
            <title>6-deoxy-β-l-talose</title>
            <link>http://scripts.iucr.org/cgi-bin/paper?lh2652</link>
            <description>X-ray crystallography showed that the title compound, C6H12O5, crystallizes in the β-pyranose form with the six-membered ring in a chair conformation. The crystal structure exists as a three-dimensional hydrogen-bonded network of molecules with each molecule acting as a donor and aceptor for three hydrogen bonds. (Source: Acta Crystallographica Section E) </description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1578283</comments>
            <pubDate>Sat, 05 Jul 2008 04:00:00 +0100</pubDate>
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