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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.
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页码:14831 / 14841
页数:11
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