HOMOLEPTIC ORGANOMETALLIC COMPOUNDS OF HEAVY PNICOGENS. CRYSTAL AND MOLECULAR STRUCTURE OF [2-(iP2NCH2)C6H4]3M (M = Sb, Bi)

被引:0
作者
Chirca, Ion [1 ]
Soran, Albert [1 ]
Silvestru, Anca [1 ]
Silvestru, Cristian [1 ]
机构
[1] Univ Babes Bolyai, Fac Chem & Chem Engn, Dept Chem, Supramol Organ & Organomet Chem Ctr SOOMCC, Cluj Napoca 400028, Romania
关键词
triorganopnicogen(III) compounds; antimony; bismuth; solution NMR spectroscopy; X-ray molecular structure; C-H ACTIVATION; OXIDATIVE ADDITION; SOLUTION BEHAVIOR; ORGANOANTIMONY(III); COMPLEXES; BOND; NCN; ANTIMONY(III); REACTIVITY; SELENIDE;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two new homoleptic triorganopnicogen(III) species, [2-((Pr2NCH2)-Pr-i)C6H4](3)M [M = Sb (2), Bi (3)] were obtained by reacting [2-((Pr2NCH2)-Pr-i)C6H4]MgBr (prepared in situ from [2-((Pr2NCH2)-Pr-i)C6H4]Br (1) and Mg filings] with MCl3. The compounds were characterized by multinuclear NMR solution studies and the crystal and molecular structure of 2 and 3 was established by single-crystal X-ray difft action. The NMR data are consistent with one type of organic group attached to the metal atom in 2 and 3. The main difference between the molecules of the organometallic species is observed in the solid state. While for the antimony(III) compound all pendant arms are twisted to push the nitrogen atoms far from the metal centre, in the bismuth(III) derivative weak intramolecular N -> Bi interactions are established for all three nitrogen atoms, thus increasing the coordination number from three to six in a distorted octahedral (C,N)(3)Bi core.
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页码:643 / 650
页数:8
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