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Distorted Germyllithium Induced by Intramolecular Coordination of an Amino Group: Synthesis and Structures of {Tris[2‐(dimethylamino)phenyl]germyl}lithium
Author(s) -
Kawachi Atsushi,
Tanaka Yoko,
Tamao Kohei
Publication year - 1999
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/(sici)1099-0682(199903)1999:3<461::aid-ejic461>3.0.co;2-l
Subject(s) - chemistry , lithium (medication) , intramolecular force , lithium atom , tris , monomer , crystallography , germanium , molecule , atom (system on chip) , phenyl group , carbon 13 nmr , stereochemistry , ion , organic chemistry , silicon , polymer , medicine , biochemistry , halogen , computer science , embedded system , ionization , endocrinology , alkyl
{Tris[2‐(dimethylamino)phenyl]germyl}lithium ( 1 ) has been prepared. The X‐ray analysis shows that 1 exists as a monochelated monomer in the solid state, where the lithium atom is coordinated to one of the amino groups and two THF molecules. The interaction between the lithium atom and the amino group induces the distortion of the geometry around the germanium atom. In solution, however, two species exist as evidenced by 1 H‐, 7 Li‐, and 13 C‐NMR spectra. The temperature‐dependent behavior of these two species has been analyzed by variable‐temperature NMR studies.

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