Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada.
J Am Chem Soc. 2015 Apr 1;137(12):4126-33. doi: 10.1021/ja512183e. Epub 2015 Mar 17.
Chalcogen bonding is the noncovalent interaction between an electron-deficient, covalently bonded chalcogen (Te, Se, S) and a Lewis base. Although substantial evidence supports the existence of chalcogen bonding in the solid state, quantitative data regarding the strengths of the interactions in the solution phase are lacking. Herein, determinations of the association constants of benzotelluradiazoles with a variety of Lewis bases (Cl(-), Br(-), I(-), NO3(-) and quinuclidine, in organic solvent) are described. The participation of the benzotelluradiazoles in chalcogen bonding interactions was probed by UV-vis, (1)H and (19)F NMR spectroscopy as well as nano-ESI mass spectrometry. Trends in the free energy of chalcogen bonds upon variation of the donor, acceptor and solvent are evident from these data, including a linear free energy relationship between chalcogen bond donor ability and calculated electrostatic potential at the tellurium center. Calculations using the dispersion-corrected B97-D3 functional were found to give good agreement with the experimental free energies of chalcogen bonding.
硫属键合是非共价相互作用,涉及缺电子的共价键硫属元素(Te、Se、S)与路易斯碱。尽管有大量证据支持固态硫属键合的存在,但溶液相相互作用强度的定量数据仍然缺乏。在此,描述了苯并噻二唑与各种路易斯碱(Cl(-)、Br(-)、I(-)、NO3(-)和奎宁啶,在有机溶剂中)的缔合常数的测定。通过紫外-可见、(1)H 和(19)F NMR 光谱以及纳米电喷雾质谱法研究了苯并噻二唑参与硫属键合相互作用的情况。从这些数据中可以明显看出硫属键自由能随供体、受体和溶剂变化的趋势,包括硫属键供体能力与碲中心计算静电势之间的线性自由能关系。使用经色散校正的 B97-D3 函数的计算结果与实验硫属键合自由能吻合良好。