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
相关论文
共 50 条
  • [1] Germylene stabilized group 12 metal complexes and their reactivity with chalcogens
    Sinhababu, Soumen
    Sharma, Mahendra Kumar
    Mahawar, Pritam
    Kaur, Supreet
    Singh, Vivek Kumar
    Paliwal, Akhil
    Yadav, Dhirendra
    Kashyape, Hemant K.
    Nagendran, Selvarajan
    DALTON TRANSACTIONS, 2019, 48 (43) : 16366 - 16376
  • [2] Lead and tin β-diketiminato amido/anilido complexes: competitive nucleophilic reactivity at the β-diketiminato γ-carbon
    Harris, Lisa A. -M.
    Tam, Eric C. Y.
    Coles, Martyn P.
    Fulton, J. Robin
    DALTON TRANSACTIONS, 2014, 43 (36) : 13803 - 13814
  • [3] Reactivity of Divalent Germanium Alkoxide Complexes Is in Sharp Contrast to the Heavier Tin and Lead Analogues
    Ferro, Lorenzo
    Hitchcock, Peter B.
    Coles, Martyn P.
    Fulton, J. Robin
    INORGANIC CHEMISTRY, 2012, 51 (03) : 1544 - 1551
  • [4] The Reactivity of Germanium Phosphanides with Chalcogens
    Harris, Lisa M.
    Tam, Eric C. Y.
    Cummins, Struan J. W.
    Coles, Martyn P.
    Fulton, J. Robin
    INORGANIC CHEMISTRY, 2017, 56 (05) : 3087 - 3094
  • [5] Synthesis and reactivity of tin amide complexes
    Harris, Lisa A. -M.
    Coles, Martyn P.
    Fulton, J. Robin
    INORGANICA CHIMICA ACTA, 2011, 369 (01) : 97 - 102
  • [6] Insights on the Reactivity of Terminal Phosphanido Metal Complexes toward Activated Alkynes from Theoretical Computations
    Alvarez, Daniel
    Mera-Adasme, Raul
    Riera, Lucia
    Cardenas-Jiron, Gloria I.
    Perez, Julio
    Diaz, Jesus
    Isabel Menendez, M.
    Lopez, Ramon
    INORGANIC CHEMISTRY, 2017, 56 (11) : 6652 - 6661
  • [7] Bridging and Terminal (Phosphanido)platinum Complexes
    Mastrorilli, Piero
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2008, 31 (31) : 4835 - 4850
  • [8] REACTIVITY OF ORGANO-TIN-PLATINUM COMPLEXES
    GLOCKLING, F
    SSEBUWUFU, PJML
    INORGANICA CHIMICA ACTA, 1978, 31 (01) : 105 - 107
  • [9] Aminotroponiminato complexes of silicon, germanium, tin and lead
    Dias, HVR
    Wang, ZY
    Jin, WC
    COORDINATION CHEMISTRY REVIEWS, 1998, 176 : 67 - 86
  • [10] Alkoxy(siloxy) complexes of tin, lead and bismuth
    Terry, KW
    Su, K
    Tilley, TD
    Rheingold, AL
    POLYHEDRON, 1998, 17 (5-6) : 891 - 897