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苯甲酸甲酯四重键合二钼配合物的晶体结构

Crystal structure of a methyl benzoate quadruple-bonded dimolybdenum complex.

作者信息

Bass Lillian Dawson, Lee Jessie H, Lilygren McKenzie C, Hartnett Alaina C, Campbell Brandon M, Morphet Daniel R, Dogutan Dilek K, Zheng Shao-Liang

机构信息

Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, 02138, USA.

出版信息

Acta Crystallogr E Crystallogr Commun. 2023 Feb 28;79(Pt 3):231-235. doi: 10.1107/S2056989023001457. eCollection 2023 Feb 1.

Abstract

Quadruple-bond dimolybdenum complexes provide invaluable insight into the two-electron bond, with structural chemistry providing a foundation for examination of bond properties. The synthesis and solid-state structure of the quadruple-bonded dimolybdenum(II) complex tetra-kis-(-4-methyl-benzoato- :')bis[(tetra-hydro-furan-κ)molybdenum(II)] tetra-hydro-furan disolvate, [Mo(CHO)(CHO)]·2CHO, are presented. This complex crystallizes in a triclinic cell with low-symmetry space group . The dimolybdenum paddlewheel structure comprises four methyl-benzoate ligands and two axial THF ligands. The dimolybdenum bond distance of 2.1012 (4) Å is exemplary of this class of compounds.

摘要

四重键二钼配合物为双电子键提供了宝贵的见解,其结构化学为研究键的性质奠定了基础。本文报道了四重键二钼(II)配合物四 - 双(-4-甲基苯甲酸根 - :')双[(四氢呋喃 - κ)钼(II)]四氢呋喃二溶剂合物[Mo(CHO)(CHO)]·2CHO的合成及其固态结构。该配合物在具有低对称空间群的三斜晶胞中结晶。二钼桨轮结构包含四个甲基苯甲酸酯配体和两个轴向四氢呋喃配体。该类化合物的二钼键距为2.1012 (4) Å。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3927/9993912/244ac7066b7f/e-79-00231-fig1.jpg

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