research papers
The hydrogen-bond acceptor ability of divalent sulfur in Y—S—Z systems, Y, Z= C, N, O or S, and the donor ability of thiol S—H have been studied using crystallographic data retrieved from the Cambridge Structural Database. Of 1811 Y—S—Z substructures that co-occur with N—H or O—H donors, only 86 (4.75%) form SH—N,O bonds within SH < 2.9 Å. In dialkylthioethers, the frequency of SH bond formation is 6.24%, but drops below 3% when the alkyl groups are successively replaced by Csp2 centres. This parallels an increasing -positivity of S as calculated using ab initio methods. A similar frequency trend is observed for OH—N,O bond formation by analogous oxyethers. Mean intermolecular >SH distances for O—H [2.67 (3) Å] and N—H [2.75 (2) Å] donors (with H positions normalized to neutron values) are ca 0.25 Å longer than in C=SH—N,O systems, indicative of very weak hydrogen bonding to >S. Intramolecular >SH are slightly more frequent (8.56%), with SH slightly shorter than for the intermolecular case. In contrast, 26 (70.3%) out of 37 S—H donors that co-occur with suitable acceptors form XH—S bonds. The C=OH—S system is predominant with a mean OH distance of 2.34 (4) Å, considerably longer (weaker) than in C=OH—O systems.