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首页> 外文期刊>Inorganica Chimica Acta >DO ORGANOCOBALT PORPHYRINS HAVE AGOSTIC ALKYL GROUPS - AN INVESTIGATION OF THE STRUCTURE OF ETHYL COBALT(III) OCTAETHYLPORPHYRIN AND THE NUCLEAR MAGNETIC RESONANCE SPECTRA OF C-13-LABELED ALKYL COBALT(III) PORPHYRIN COMPLEXES
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DO ORGANOCOBALT PORPHYRINS HAVE AGOSTIC ALKYL GROUPS - AN INVESTIGATION OF THE STRUCTURE OF ETHYL COBALT(III) OCTAETHYLPORPHYRIN AND THE NUCLEAR MAGNETIC RESONANCE SPECTRA OF C-13-LABELED ALKYL COBALT(III) PORPHYRIN COMPLEXES

机译:有机脂卟啉是否具有农业烷基基团-乙基钴(III)乙基卟啉的结构和C-13标记的烷基钴(III)卟啉的核磁共振谱的研究

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The X-ray structure of Co(OEP)Et and the H-1 and C-13 NMR spectroscopy of Co(P)R, where R = alkyl and P = OEP, TTP, OEC and OEiBC, were investigated to determine whether evidence supports the existence of the agostic interaction that had been postulated to explain the anomalous features of the compounds' NMR spectra. Co(OEP)Et, C38H49CoN4, crystallized in the triclinic space group P (1) over bar (Z=2) with unit cell dimensions a = 10.675(1), b = 10.886(1), c = 13.973(1) Angstrom, alpha = 79.539(8), beta = 86.386(7), gamma = 79.298(8)degrees, and V = 1568.2(2) Angstrom(3) at 173(2) K. The structural features of the ordered axial ethyl group were inconsistent with an agostic interaction in the solid state. Synthesis and use of C-13-labeled compounds were necessary to observe the C-13 NMR spectra of the axial alkyl groups and to measure informative coupling constants. The C-13 resonances of carbons bound to cobalt were quite broad and had unusual upheld shifts. Coordination of pyridine as a trans axial ligand narrowed the linewidth of the cw-carbon resonance and caused it to move significantly downfield. The spectroscopic data were inconsistent with an agostic interaction in solution. The anomalous features of the NMR spectra were ascribed to the effects of the quadrupolar Co-59 nucleus and to paramagnetic contact shifts that arise from thermal population of an excited state. (C) 1997 Elsevier Science S.A. [References: 45]
机译:研究Co(OEP)Et的X射线结构以及Co(P)R的H-1和C-13 NMR光谱,其中R =烷基,P = OEP,TTP,OEC和OEiBC,以确定是否有证据支持推测了解释化合物NMR光谱异常特征的异常相互作用的存在。 Co(OEP)Et,C38H49CoN4,在晶格空间群P(1)上的晶格(Z = 2)上结晶,晶胞尺寸为a = 10.675(1),b = 10.886(1),c = 13.973(1)埃,α= 79.539(8),β= 86.386(7),γ= 79.298(8)度,在173(2)K时V = 1568.2(2)埃(3)。有序轴向乙基的结构特征与固态中的不良互动不一致。合成和使用C-13标记的化合物对于观察轴向烷基的C-13 NMR光谱和测量信息偶联常数是必要的。与钴结合的碳原子的C-13共振非常宽泛,并且具有异常的维持位移。吡啶作为反式轴向配位体的配位使顺时针-碳共振的线宽变窄,并导致其大幅向低场移动。光谱数据与溶液中的有害相互作用不一致。 NMR谱的异常特征归因于四极Co-59核的影响以及由于激发态的热填充引起的顺磁接触位移。 (C)1997 Elsevier Science S.A. [参考:45]

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