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具有非常大偶极矩的金属配合物:阴离子碳硼烷腈12-NC-CB11X11(-)(X = H、F、CH3)作为Pt(II)和Pd(II)上的配体

Metal Complexes with Very Large Dipole Moments: the Anionic Carborane Nitriles 12-NC-CB11X11(-) (X = H, F, CH3) as Ligands on Pt(II) and Pd(II).

作者信息

Šembera Filip, Plutnar Jan, Higelin Alexander, Janoušek Zbyněk, Císařová Ivana, Michl Josef

机构信息

Institute of Organic Chemistry and Biochemistry AS CR, v.v.i. , Flemingovo nám. 2, 16610 Prague, Czech Republic.

Department of Inorganic Chemistry, Charles University , Hlavova 2030, 12843 Prague 2, Czech Republic.

出版信息

Inorg Chem. 2016 Apr 18;55(8):3797-806. doi: 10.1021/acs.inorgchem.5b02678. Epub 2016 Mar 28.

DOI:10.1021/acs.inorgchem.5b02678
PMID:27018918
Abstract

The anionic nitriles 1-R-12-NC-CB11H10(-) (R = H, CH3, I, COOH), 12-NC-1-H-CB11Me10(-), and 12-NC-1-H-CB11F10(-) were prepared, and three of them were examined for complex formation with (Et3P)2Pt(II) and (Et3P)2Pd(II). Several stable internally charge-compensated zwitterionic complexes were obtained and characterized. RI-BP86/SV(P) calculations suggest that their dipole moments exceed 20 D. An attempt to measure the dipole moments in solution failed due to insufficient solubility in solvents of low polarity.

摘要

制备了阴离子腈1-R-12-NC-CB11H10(-)(R = H、CH3、I、COOH)、12-NC-1-H-CB11Me10(-)和12-NC-1-H-CB11F10(-),并对其中三种与(Et3P)2Pt(II)和(Et3P)2Pd(II)形成配合物的情况进行了研究。获得并表征了几种稳定的内部电荷补偿两性离子配合物。RI-BP86/SV(P)计算表明它们的偶极矩超过20 D。由于在低极性溶剂中的溶解度不足,未能成功测量溶液中的偶极矩。

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