You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/39052
Title: 
Small angle X-ray scattering and IR spectroscopy study of metal carbonyl complexes immobilized on a silica gel surface chemically modified with piperazine
Author(s): 
Institution: 
  • Universidade Federal do Rio Grande do Sul (UFRGS)
  • Universidade Estadual Paulista (UNESP)
ISSN: 
0277-5387
Abstract: 
The carbonyl complexes [WCl(CO)(3)(bipy) (HgCl)] (1), [Fe(CO)(4)(HgCl)(2)] (2) and W(CO)(6)] (3) were immobilized on a silica gel surface organofunctionalized with piperazine groups. The products obtained were studied by IR spectroscopy and small angle X-ray scattering (SAXS) techniques. The IR data show that the immobilization of heterobimetallic compounds 1 and 2, on the functionalized surface, occurred through the mercury atom, while for 3 the displacement of one CO group by the nitrogen of a piperazine molecule was observed. The data obtained from SAXS indicate that particles have a uniform size and reveal suitable modifications on the functionalized surface after immobilization of metal carbonyl complexes. The average intermolecular distance (l(ij)) for piperazine ligands on support is 8.7 Angstrom, for the metal carbonyl complex 1 it is 18.8 Angstrom, for complex 2 it is 16.2 Angstrom and for complex 3 it is 15.3 Angstrom. Copyright (C) 1996 Elsevier B.V. Ltd
Issue Date: 
1-Jan-1996
Citation: 
Polyhedron. Oxford: Pergamon-Elsevier B.V., v. 15, n. 23, p. 4179-4183, 1996.
Time Duration: 
4179-4183
Publisher: 
Elsevier B.V.
Keywords: 
  • metal carbonyl
  • immobilization
  • silica gel
  • piperazine
  • infrared spectroscopy
  • small angle X-ray scattering
Source: 
http://dx.doi.org/10.1016/0277-5387(96)00174-X
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/39052
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.