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A Borane Platinum Complex Undergoing Reversible Hydride Migration in Solution
Inorganic Chemistry ( IF 4.6 ) Pub Date : 2018-01-16 00:00:00 , DOI: 10.1021/acs.inorgchem.7b02807
Abdollah Neshat 1 , Hamid R. Shahsavari 1 , Piero Mastrorilli 2 , Stefano Todisco 2 , Mohsen Golbon Haghighi 3 , Behrouz Notash 3
Affiliation  

Reaction of [Pt(κ2-C,N-ppy)(dmso)Cl], 1 (Hppy = 2-phenylpyridine), with Na[H2B(mb)2] (Hmb = 2-mercapto-benzimidazole) smoothly afforded the complex {[(κ3-S,B,S-HB(mb)2]Pt(κ2-C,N-ppy)H}, 2, featuring a strong reverse-dative Pt → B σ interaction in the solid state. When dissolved in thf (or acetone) solution, 2 undergoes a reversible Pt–H bond activation, establishing an equilibrium between the hexacoordinated 2 and the tetracoordinate complex {[(κ2-S,S-H2B(mb)2]Pt(κ2-C,N-ppy)}, 3, as ascertained by multinuclear NMR. Hydrolysis of the B–N bond in 2/3 resulted ultimately in the formation of a dimeric half-lantern platinum(II,II) complex [{Pt(κ2-C,N-ppy)(μ22-N,S-mb)}2], 4. The SC-XRD structures of 2 and 4 are reported.

中文翻译:

硼烷铂络合物在溶液中经历可逆氢化物迁移

的反应[PT(κ 2 - çÑ -ppy)(DMSO)CL],1(Hppy = 2-苯基吡啶),用Na [H 2 B(MB)2 ](管柱= 2-巯基苯并咪唑)顺利得到络合物{[(κ 3 -小号小号-HB(MB)2 ]的Pt(κ 2 - çñ -ppy)H},2,具有在一个强的反向配价的Pt→乙σ相互作用当溶解在thf(或丙酮)溶液中时,2经历可逆的Pt-H键活化,在六配位的2之间建立平衡和四配位配合物{[(κ 2 -小号小号-H 2 B(MB)2 ]的Pt(κ 2 - çÑ -ppy)},3,如确定由多核NMR的B-N键的水解。在2 / 3最终导致形成二聚体半灯笼铂(II,II)配合物[{的Pt(κ 2 - çñ -ppy)(μ 22 - ñ小号-MB)} 2 ] 4。的SC-XRD结构2报告了4个
更新日期:2018-01-16
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