Tin and Lead Phosphanido Complexes: Reactivity with Chalcogens

被引:5
|
作者
Tam, Eric C. Y. [1 ]
Apperley, David C. [2 ]
Smith, J. David [1 ]
Coles, Martyn P. [1 ,3 ]
Fulton, J. Robin [1 ,3 ]
机构
[1] Univ Sussex, Dept Chem, Brighton BN1 9QJ, E Sussex, England
[2] Univ Durham, Dept Chem, South Rd, Durham DH1 3LE, England
[3] Victoria Univ Wellington, Sch Chem & Phys Sci, POB 600, Wellington 6012, New Zealand
关键词
X-RAY CRYSTAL; MOLECULAR-STRUCTURE; COORDINATION CHEMISTRY; MULTIPLE BONDS; MAIN-GROUP; SE; GERMANIUM; SN; TIN(II); TE;
D O I
10.1021/acs.inorgchem.7b02040
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reactivity of tin and lead phosphanido complexes with chalogens is reported. The addition of sulfur to [(BDI)MPCy2] (M = Sn, Pb; BDI = CH{(CH3)CN-2,6-iPr(2)C(6)H(3)}(2)) results in the formation of phosphinodithioates [(BDI)MSP(S)Cy-2] regardless of the conditions; however, when selenium is added to [(BDI)MPCy2], a selenium insertion product, phosphinoselenoite [(BDI)MSePCy2], can be isolated. This compound readily reacts with additional selenium to form the phosphinodiselenoate complex [(BDI)MSeP(Se)Cy-2]. In contrast, the addition of selenium to [(BDI)SnP(SiMe3)(2)] results in the formation of the heavy ether [(BDI)SnSeSiMe3]. Differences in the solution and solid-state molecular species of tin phosphinoselenoite and phosphinodiselenoate complexes were probed :using multinudear solution and solid-state NMR spectroscopy.
引用
收藏
页码:14831 / 14841
页数:11
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