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Reactions of Dilithium Dibenzopentalenides with Cr(CO) 3 (CH 3 CN) 3 : Unexpected Formation of a Cubic Tetramer of an Anionic Hydrodibenzopentalenyl Complex
Author(s) -
Kuwabara Takuya,
Kurokawa Nobuaki,
Saito Masaichi
Publication year - 2017
Publication title -
chempluschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.801
H-Index - 61
ISSN - 2192-6506
DOI - 10.1002/cplu.201700043
Subject(s) - chemistry , dilithium , tetramer , lithium (medication) , crystallography , silylation , dimer , chromium , medicinal chemistry , pentalene , stereochemistry , molecule , organic chemistry , catalysis , medicine , ion , deprotonation , enzyme , endocrinology
To explore the coordination chemistry of dibenzopentalene dianion, reactions of two dilithium dibenzopentalenides having different silyl substituents with Cr(CO) 3 (CH 3 CN) 3 were investigated. The products were unexpected anionic complexes, [Li(Et 2 O)] + [Cr( η 5 ‐9‐hydrodibenzopentalenyl)(CO) 3 ] − . The proton at the 9‐position is derived from Cr(CO) 3 (CH 3 CN) 3 , as evidenced by the use of Cr(CO) 3 (CD 3 CN) 3 . The X‐ray diffraction analysis revealed that the chromium is coordinated by an anionic five‐membered ring of the pentalene skeleton, and the lithium atom is coordinated by oxygen atoms of the carbonyl groups. The complexes form a dimer or a cage‐like tetramer via carbonyl–lithium interactions, depending on the bulk of the silyl groups. The cubic tetramer appears to retain its cage structure in nonpolar solvents such as benzene.