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  - 

@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}
}