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Configurational rearragements in cis-M(AA)2X2, cis-M(AA)2XY, and cis-M(AB)2X2 complexes. 4. The cis-M(AA)2X2 system: Ti(3-iC3H7-acac)2Cl2

✍ Scribed by D.G. Bickley; N. Serpone


Book ID
104138331
Publisher
Elsevier Science
Year
1977
Tongue
English
Weight
308 KB
Volume
25
Category
Article
ISSN
0020-1693

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✦ Synopsis


In a preceding paper [l] we reported the results of incorporating a diasterotopic isopropyl group at the terminal AA positions of complexes of the type cis-M(AA)zXz.

It was argued, on permutational grounds, that the steric course of the configurational changes in these &-type complexes can be rationalized in terms of the As averaging set [2]. Placement of the prochiral isopropyl group in the y-or (3-) position of the acetylacetonate (acac) ring in a M(AA)2X2 complex can, in principle, provide an opportunity to study the environmental averaging of terminal A groups, and the inversion of the molecular configuration independently.

The present work reports on our investigations of the configurational changes taking place in the complex Ti(3-l&H,-acac)&lz using the variable temperature nuclear magnetic resonance method.


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Pd(II) and Pt(II) complexes of [16]aneS 4 and Pd(II) complexes of cis-(HO) 2 [14]aneS 4 and [9]aneS 3 have been used as templates for the selfassembly of polyiodide ions. The complexes {[M([16]aneS 4 )] 2 I}I 11 (M Ο­ Pd, Pt), [Pd(cis-(HO) 2 [14]aneS 4 )](I 3 ) 2 , [Pd([9]aneS 3 ) 2 ](I x ) 2 (x Ο­ 3,