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首页> 外文期刊>Journal of chemical crystallography >Complexes of Ambidentate N,O-Donor Ligands with Rhenium(I) and -(V)
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Complexes of Ambidentate N,O-Donor Ligands with Rhenium(I) and -(V)

机译:与铼(I)和 - (v)的外壳n

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摘要

The reaction of the potentially bidentate ambidentate N,O-donor ligands 3-hydroxy-2-pyridinecarboxylic acid (Hhpc) and 3-hydroxy-2-(hydroxymethyl)pyridine (Hhhp) with trans -[ReOCl~(3)(PPh~(3))~(2)] led to the isolation of the products [ReOCl(hpc)~(2)] ( 1 ) (from acetonitrile) and [ReOCl~(2)(hhp)(PPh~(3))] ( 2 ) (from ethanol) respectively. In both complexes hpc and hhp are coordinated as bidentate N,O-donor chelates, rather than as O,O-donor ligands. From the reaction of [Re(CO)~(5)Cl] and Hhhp·HCl in ethanol the neutral complex fac -[Re(CO)~(3)Cl(Hhhp)] ( 3 ) was obtained, with N,O-coordination of Hhhp. Complex 1 crystallizes in the monoclinic space group P 2~(1)/n with a ?=?6.8782(3), b ?=?20.0647(8), c ?=?10.8692(4)??, β ?=?107.545(1)°, and Z ?=?4. Complex 2 crystallizes in the triclinic space group P -1 with a ?=?7.3523(4), b ?=?8.1047(5), c ?=?19.591(1)??, α ?=?91.133(2)°, β ?=?93.656(2)°, γ ?=?93.074(2)° and Z ?=?2. Complex 3 has monoclinic P 2~(1)/c symmetry with the cell parameters a ?=?10.6452(5), b ?=?11.1372(5), c ?=?9.7229(5)??, β ?=?106.107(2)°, and Z ?=?4. Graphical Abstract The reaction of the potentially bidentate ambidentate N,O-donor ligands 3-hydroxy-2-pyridinecarboxylic acid (Hhpc) and 3-hydroxy-2-(hydroxymethyl)pyridine (Hhhp) with trans -[ReOCl~(3)(PPh~(3))~(2)] led to the isolation of the products [ReOCl(hpc)~(2)] (from acetonitrile) and [ReOCl~(2)(hhp)(PPh~(3))] (from ethanol) respectively. In both complexes hpc and hhp are coordinated as bidentate N,O-donor chelates, rather than as O,O-donor ligands. From the reaction of [Re(CO)~(5)Cl] and Hhhp·HCl in ethanol the neutral complex fac -[Re(CO)~(3)Cl(Hhhp)] was obtained, with N,O-coordination of Hhhp. Spectroscopic data and the X-ray crystal structures of the complexes are reported.
机译:将潜在的双齿的反应绝缘N,O-供体配体3-羟基-2-吡啶羧酸(HHPC)和3-羟基-2-(羟甲基)吡啶(HHHP)用反式 - [Reocl〜(3)(PPH〜 (3))〜(2)]导致产物[Reocl(HPC)〜(2)](1)(来自乙腈)和[Reocl〜(2)(HHP)(PPH〜(3)) ](2)(来自乙醇)。在络合物中,HPC和HHP协调为二齿N,O-供体螯合物,而不是作为O-供体配体。从[Re(CO)〜(5)Cl]和HHHP·HCl在乙醇中的反应中,获得中性复合物 - [Re(CO)〜(3)Cl(HHHP)](3),用N,O - HHHP的协调。复合物1用α=Δ6.8782(3),B?= 20.0647(8),c?β= ??,β=? 107.545(1)°和z?=?4。复合物2用α=α=α=α=α=α=α.=α.8.1047(5),C?= 19.591(1)??,α?=α91.133(2)° ,β?= 93.656(2)°,γ?=α= 93.074(2)°和z?=?2。复合物3具有单斜晶型p 2〜(1)/ c对称性与细胞参数a?=α= 10.6452(5),b?= 11.1372(5),c?= 9.7229(5)??,β?=? 106.107(2)°和z?=?4。图形摘要潜在的二齿的绝缘N,O-供体配体3-羟基-2-吡啶羧酸(HHPC)和3-羟基-2-(羟甲基)吡啶(HHHP)的反应 - [Reocl〜(3)( PPH〜(3))〜(2)]导致产物[REOCL(HPC)〜(2)](来自乙腈)和[再克〜(2)(HHP)(PPH〜(3))]] (来自乙醇)。在络合物中,HPC和HHP协调为二齿N,O-供体螯合物,而不是作为O-供体配体。从[Re(CO)〜(5)Cl]和HHHP·HCl在乙醇中的反应中,获得中性复合物 - [Re(CO)〜(3)Cl(HHHP)],N,O-协调HHHP。报道了复合物的光谱数据和X射线晶体结构。

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