Digital Repository

Thiazole–Carbonyl Interactions: A Case Study Using Phenylalanine Thiazole Cyclic Tripeptides

Show simple item record

dc.contributor.author MALI, SACHITANAND M. en_US
dc.contributor.author Schneider, Tobias F. en_US
dc.contributor.author BANDYOPADHYAY, ANUPAM en_US
dc.contributor.author JADHAV, SANDIP V. en_US
dc.contributor.author Werz, Daniel B. en_US
dc.contributor.author GOPI, HOSAHUDYA N. en_US
dc.date.accessioned 2019-07-23T11:08:16Z
dc.date.available 2019-07-23T11:08:16Z
dc.date.issued 2012-09 en_US
dc.identifier.citation Crystal Growth & Design, 12(11), 5643-5648. en_US
dc.identifier.issn 1528-7483 en_US
dc.identifier.issn 1528-7505 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3608
dc.identifier.uri https://doi.org/10.1021/cg301147s en_US
dc.description.abstract Natural as well as synthetic thiazole/oxazole peptides have shown widespread pharmacological and metal binding properties. Herein, phenylalanine- and tyrosine derived thiazole-containing cyclic tripeptides were synthesized, and the influence of the solvent on the supramolecular assembly in the solid state was investigated. Striking influences of the solvent on the solid state structure were observed. S···O interactions between the sulfur of a thiazole ring and a carbonyl moiety of an amide showing an average distance of 3.1 Å which is much smaller than the sum of the van der Waals radii predominantly mediate the crystal structure. To get deeper insights into this kind of interaction, two model systems consisting of thiazole and acetyl-N-methylamide were studied using the MP2/6-311G++(3df,3dp) level of theory. Theoretical calculations revealed that these interactions are associated with an average energy gain of about 16 kJ/mol in comparison with the separated species. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Chemistry en_US
dc.subject 2012 en_US
dc.title Thiazole–Carbonyl Interactions: A Case Study Using Phenylalanine Thiazole Cyclic Tripeptides en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Crystal Growth & Design en_US
dc.publication.originofpublisher Foreign en_US


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search Repository


Advanced Search

Browse

My Account