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含PhP(CH(2)CH(2)CH(2)PCy(2))(2)(Cyttp)的铼多氢配合物:ReH(5)(Cyttp)的质子化、插入和配体取代反应以及ReH(5)(Cyttp)和[ReH(4)(η(2)-H(2))(Cyttp)]SbF(6)的结构表征

Rhenium Polyhydride Complexes Containing PhP(CH(2)CH(2)CH(2)PCy(2))(2) (Cyttp): Protonation, Insertion, and Ligand Substitution Reactions of ReH(5)(Cyttp) and Structural Characterization of ReH(5)(Cyttp) and [ReH(4)(eta(2)-H(2))(Cyttp)]SbF(6).

作者信息

Kim Youhyuk, Deng Haibin, Gallucci Judith C., Wojcicki Andrew

机构信息

Departments of Chemistry, The Ohio State University, Columbus Ohio 43210, and Dankook University, 29 Anseo Dong, Cheonan, Choongnam 330-714, South Korea.

出版信息

Inorg Chem. 1996 Nov 20;35(24):7166-7173. doi: 10.1021/ic9602714.

Abstract

Several new polyhydride complexes of rhenium containing the tridentate phosphine PhP(CH(2)CH(2)CH(2)PCy(2))(2) (Cyttp) were synthesized and characterized by (1)H and (31)P{(1)H} NMR and IR spectroscopy. The solid state structure of the previously reported ReH(5)(Cyttp) (1) was determined by X-ray crystallography. 1 crystallizes in the space group P2(1)/m with the following unit cell parameters: a = 8.582(2) Å, b = 19.690(2) Å, c = 10.800(2) Å, beta = 95.57(1) degrees, and Z = 2. The molecule adopts a classical polyhydride, triangulated dodecahedral structure, with the three phosphorus atoms and one hydrogen atom occupying the B sites, and the remaining hydrogen atoms occupying the A sites. 1 is protonated by HSbF(6) (or HBF(4)) to yield [ReH(4)(eta(2)-H(2))(Cyttp)]SbF(6) (3), which was shown by X-ray diffraction techniques (space group P&onemacr;, unit cell parameters: a = 9.874(2) Å, b = 14.242(4) Å, c = 16.198(2) Å, alpha = 99.12(2) degrees, beta = 98.85(2) degrees, gamma = 109.42(2) degrees, and Z = 2) to contain a nonclassical polyhydride cation with a triangulated dodecahedral structure in the solid. The same structure is suggested in solution by (1)H NMR data (including T(1) measurements). 3 is inert to loss of H(2) and is unaffected by CO, t-BuNC, and P(OMe)(3) at room temperature. In contrast, 1 reacts with a variety of reagents to afford classical tetrahydride complexes which are thought also to possess a triangulated dodecahedral structure, with the hydrogens in the A sites, from spectroscopic evidence. Accordingly, CS(2), p-O(2)NC(6)H(4)NCS, and EtOC(O)NCS (X=C=S) insert into an Re-H bond to yield ReH(4)(SCH=X)(Cyttp) (5-7, respectively). MeI cleaves one Re-H bond to afford ReH(4)I(Cyttp) (8), and [C(7)H(7)]BF(4) abstracts hydride in the presence of MeCN, t-BuNC, CyNC, or P(OMe)(3) (L) to give [ReH(4)L(Cyttp)]BF(4) (9-12, respectively). A related pentahydride, ReH(5)(ttp) (2, ttp = PhP(CH(2)CH(2)CH(2)PPh(2))(2)), also reacts with HSbF(6) to yield [ReH(6)(ttp)]SbF(6) (4), which appears to be a nonclassical polyhydride in solution by T(1) measurements.

摘要

合成了几种含三齿膦PhP(CH(2)CH(2)CH(2)PCy(2))(2)(Cyttp)的新型铼多氢化物配合物,并通过(1)H和(31)P{(1)H}核磁共振以及红外光谱对其进行了表征。通过X射线晶体学确定了先前报道的ReH(5)(Cyttp)(1)的固态结构。1结晶于空间群P2(1)/m中,晶胞参数如下:a = 8.582(2) Å,b = 19.690(2) Å,c = 10.800(2) Å,β = 95.57(1)°,Z = 2。该分子采用经典的多氢化物三角十二面体结构,三个磷原子和一个氢原子占据B位,其余氢原子占据A位。1被HSbF(6)(或HBF(4))质子化生成[ReH(4)(η(2)-H(2))(Cyttp)]SbF(6)(3),通过X射线衍射技术(空间群P&onemacr;,晶胞参数:a = 9.874(2) Å,b = 14.242(4) Å,c = 16.198(2) Å,α = 99.12(2)°,β = 98.85(2)°,γ = 109.42(2)°,Z = 2)表明其在固态中含有具有三角十二面体结构的非经典多氢化物阳离子。(1)H核磁共振数据(包括T(1)测量)表明溶液中也具有相同结构。3对H(2)的损失呈惰性,在室温下不受CO、t-BuNC和P(OMe)(3)的影响。相比之下,1与多种试剂反应生成经典的四氢化物配合物,根据光谱证据推测这些配合物也具有三角十二面体结构,氢原子位于A位。因此,CS(2)、p-O(2)NC(6)H(4)NCS和EtOC(O)NCS(X = C = S)插入到Re-H键中生成ReH(4)(SCH = X)(Cyttp)(分别为5 - 7)。MeI切断一个Re-H键生成ReH(4)I(Cyttp)(8),[C(7)H(7)]BF(4)在MeCN、t-BuNC、CyNC或P(OMe)(3)(L)存在下夺取氢化物生成[ReH(4)L(Cyttp)]BF(4)(分别为9 - 12)。一种相关的五氢化物ReH(5)(ttp)(2,ttp = PhP(CH(2)CH(2)CH(2)PPh(2))(2))也与HSbF(6)反应生成[ReH(6)(ttp)]SbF(6)(4),通过T(1)测量表明其在溶液中似乎是一种非经典多氢化物。

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