IRIS publication 57685675
Sulfoxides: Potent Co-Crystal Formers
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TY - JOUR - Eccles, Kevin S.,Elcoate, Curtis J.,Stokes, Stephen P.,Maguire, Anita R.,Lawrence, Simon E. - 2010 - October - Crystal Growth ; Design - Sulfoxides: Potent Co-Crystal Formers - Validated - () - 10 - 10 - 4243 - 4245 - The design of co-crystals requires knowledge of robust supramol. synthons. The sulfoxide is a potent H bond acceptor and was used as a co-crystal former with a range of NH functional groups, via N-H···O=S H bonds. The NH functional group retains favorable H bond motifs from its own structure in all cases where this is possible, with the sulfoxide interacting in a discrete, capping fashion in four cases and in a bifurcated, bridging fashion in the three other cases presented here. Crystallog. data are given for 7 co-formers, dibenzyl sulfoxide and cyclohexanecarbothioamide. - 1528-7483 DA - 2010/10 ER -
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@article{V57685675, = {Eccles, Kevin S. and Elcoate, Curtis J. and Stokes, Stephen P. and Maguire, Anita R. and Lawrence, Simon E. }, = {2010}, = {October}, = {Crystal Growth ; Design}, = {Sulfoxides: Potent Co-Crystal Formers}, = {Validated}, = {()}, = {10}, = {10}, pages = {4243--4245}, = {{The design of co-crystals requires knowledge of robust supramol. synthons. The sulfoxide is a potent H bond acceptor and was used as a co-crystal former with a range of NH functional groups, via N-H···O=S H bonds. The NH functional group retains favorable H bond motifs from its own structure in all cases where this is possible, with the sulfoxide interacting in a discrete, capping fashion in four cases and in a bifurcated, bridging fashion in the three other cases presented here. Crystallog. data are given for 7 co-formers, dibenzyl sulfoxide and cyclohexanecarbothioamide.}}, issn = {1528-7483}, source = {IRIS} }
Data as stored in IRIS
AUTHORS | Eccles, Kevin S.,Elcoate, Curtis J.,Stokes, Stephen P.,Maguire, Anita R.,Lawrence, Simon E. | ||
YEAR | 2010 | ||
MONTH | October | ||
JOURNAL_CODE | Crystal Growth ; Design | ||
TITLE | Sulfoxides: Potent Co-Crystal Formers | ||
STATUS | Validated | ||
TIMES_CITED | () | ||
SEARCH_KEYWORD | |||
VOLUME | 10 | ||
ISSUE | 10 | ||
START_PAGE | 4243 | ||
END_PAGE | 4245 | ||
ABSTRACT | The design of co-crystals requires knowledge of robust supramol. synthons. The sulfoxide is a potent H bond acceptor and was used as a co-crystal former with a range of NH functional groups, via N-H···O=S H bonds. The NH functional group retains favorable H bond motifs from its own structure in all cases where this is possible, with the sulfoxide interacting in a discrete, capping fashion in four cases and in a bifurcated, bridging fashion in the three other cases presented here. Crystallog. data are given for 7 co-formers, dibenzyl sulfoxide and cyclohexanecarbothioamide. | ||
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ISBN_ISSN | 1528-7483 | ||
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