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author:

Jian, G. (Jian, G..) [1] | Kaiqiang, W. (Kaiqiang, W..) [2] | Lili, X. (Lili, X..) [3] | Fengbo, X. (Fengbo, X..) [4] | Yaofeng, Y. (Yaofeng, Y..) [5]

Indexed by:

Scopus PKU CSCD

Abstract:

Polypyridyl ruthenium (II) complexes exhibit unique photophysical, photochemical, electrochemical, electron transfer, energy transfer, molecular assembly and molecular recognition properties. Ferrocenyl group has many attractive features, such as excellent reversible redox properties, high solubility in organic media, and high modifiability by organic synthesis methods, and its derivatives remain those distinguish properties in the applications of functional molecules. The ferrocenyl-functionalized terpyridine ligands are particularly interesting, since this type of ligand displays a high binding affinity to many metal ions, offering the thermodynamic driving force for stable metallosupramolecule formation. Furthermore, these ligands can be used for the construction of geometrically well-defined functional complexes which show fascinating properties based on intramolecular electron and energy transfer. This review focuses on the research progress of ferrocenyl- functionalized ruthenium(II) terpyridine complexes, specially those containing extensively conjugated ferrocenylethynyl and ferrocenylphenylethynyl substituents. Combined with our research results, optoelectronic property alterations of this class of compounds arosed by the introduction, number variation (one or two) and position isomerization of alkynyl are discussed.

Keyword:

Charge transfer; Ferrocenyl; Optoelectronic molecules; Ruthenium (II) terpyridine complexes

Community:

  • [ 1 ] [Jian, G.]State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 2 ] [Kaiqiang, W.]State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 3 ] [Lili, X.]State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 4 ] [Fengbo, X.]State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China
  • [ 5 ] [Yaofeng, Y.]State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 6 ] [Yaofeng, Y.]State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, China

Reprint 's Address:

  • [Yaofeng, Y.]State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China

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Source :

Progress in Chemistry

ISSN: 1005-281X

Year: 2010

Issue: 5

Volume: 22

Page: 773-783

0 . 5 6

JCR@2010

1 . 0 0 0

JCR@2023

JCR Journal Grade:4

CAS Journal Grade:4

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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