Journal
COORDINATION CHEMISTRY REVIEWS
Volume 257, Issue 23-24, Pages 3192-3201Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2013.03.015
Keywords
Coinage metals; Main group metals; Amidinates; Guanidinates; Iminopyrrolidinates; Thermolysis; Chemical vapor deposition; Atomic layer deposition
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The thermolysis of metal compounds incorporating amidinate-type ligands (RN(H)C(X)NR, where R is any alkyl and X is an alkyl or an amido) show a great complexity and diversity. Amidinates and guanidinates of copper(I), aluminium(III) and gallium(III) can undergo thermal decomposition by two main routes: elimination of carbodiimide (here called deinsertion) and by abstraction of a beta-hydrogen. In general terms carbodiimide deinsertion tends to be a low temperature and solution-based thermolysis route, and beta-hydrogen elimination tends to be a high temperature and gas phase thermolysis path. There is little difference between amidinates and guanidiantes in this respect: both ligands show these decomposition pathways on a variety of metal centres. The iminopyrrolidinate (ip) ligand can be designed without beta-hydrogens, and so the ligand tert-butyl-imino-2,2-dimethylpyrrolidinate (Bu-t-ip) was used on copper(I) to successfully show that this compound does not undergo these two thermolyses, but undergoes a much higher thermolysis through loss of the iminotertbutyl group and subsequent decomposition of the five-membered ring. This redesigned ligand boosts the thermal stability of the copper(I) dimer from 225 degrees C for [CuI((iPrN)2CNMe2}](2) to 350 degrees C for [Cu-1(Me-2-Bu-t-iP)](2). (C) 2013 Elsevier B.V. All rights reserved.
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