Abstract
Some aspects of the reactivity of sulfur(II) compounds—specially of N,N'-thiobisamines, toward hydrolysis, alcoholysis. and formation of coordination compounds—are discussed using experimental and theoretical results. Frontier molecular oribitals obtained from CNDO/2 calculations including sulfur d orbitals for a set of representative sulfur(II) species show that the reactivities of these compounds. following the series:
[Me2NSNHMe2]+ > S(OH)2 > SCl2 > neutral thiobisamines > thiobisphthalimide. are adequately described by considering both charge and orbital effects.