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Volumn 119, Issue 40, 1997, Pages 9550-9557

Synthesis, characterization, optical spectroscopic, electronic structure, and second-order nonlinear optical (NLO) properties of a novel class of donor-acceptor bis(salicylaldiminato)nickel(II) Schiff base NLO chromophores

Author keywords

[No Author keywords available]

Indexed keywords

LIGAND; METAL COMPLEX; ORGANOMETALLIC COMPOUND; SCHIFF BASE;

EID: 0030732057     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja971349y     Document Type: Article
Times cited : (304)

References (64)
  • 1
    • 9844268900 scopus 로고
    • Lindsay, G. A., Singer, K. D., Eds.; ACS Symposium Series 601; American Chemical Society: Washington, DC
    • (a) Polymers for Second-Order Nonlinear Optics; Lindsay, G. A., Singer, K. D., Eds.; ACS Symposium Series 601; American Chemical Society: Washington, DC, 1995.
    • (1995) Polymers for Second-Order Nonlinear Optics
  • 2
    • 0004173645 scopus 로고
    • Zyss, J., Ed.; Academic Press: New York
    • (b) Molecular Nonlinear Optics; Zyss, J., Ed.; Academic Press: New York, 1994.
    • (1994) Molecular Nonlinear Optics
  • 4
    • 9844255448 scopus 로고
    • Marder, S. R., Sohn, J. E., Stucky, G. D., Eds.; ACS Symposium Series 455; American Chemical Society: Washington, DC
    • (d) Materials for Nonlinear Optics: Chemical Perspectives; Marder, S. R., Sohn, J. E., Stucky, G. D., Eds.; ACS Symposium Series 455; American Chemical Society: Washington, DC, 1991.
    • (1991) Materials for Nonlinear Optics: Chemical Perspectives
  • 6
    • 0003551754 scopus 로고    scopus 로고
    • Khoo, I. C., Simoni, F., Umeton, C., Eds; John Wiley & Sons: New York
    • For recent reviews on NLO materials see, for example: (a) Ledoux, I.; Zyss, J. In Novel Optical Materials and Applications; Khoo, I. C., Simoni, F., Umeton, C., Eds; John Wiley & Sons: New York, 1997.
    • (1997) Novel Optical Materials and Applications
    • Ledoux, I.1    Zyss, J.2
  • 11
    • 85010917178 scopus 로고    scopus 로고
    • (d) Optical Nonlinearities in Chemistry; Burland, D. M., Ed., Chem. Rev. 1994, 94 (no. 1), 1-278.
    • (1994) Chem. Rev. , vol.94 , Issue.1 , pp. 1-278
    • Burland, D.M.1
  • 13
    • 0003423451 scopus 로고
    • Hann, R, A., Bloor, D., Eds.; Royal Society of Chemistry: London.
    • (b) Organic Materials for Nonlinear Optics III; Hann, R, A., Bloor, D., Eds.; Royal Society of Chemistry: London. 1992.
    • (1992) Organic Materials for Nonlinear Optics III
  • 14
    • 0003423449 scopus 로고
    • Hann, R. A., Bloor, D., Eds.; Royal Society of Chemistry: London
    • (c) Organic Materials for Nonlinear Optics II; Hann, R. A., Bloor, D., Eds.; Royal Society of Chemistry: London, 1991.
    • (1991) Organic Materials for Nonlinear Optics II
  • 15
    • 0003423445 scopus 로고
    • Messier, J., Kajzar, F., Prasad, P., Eds.; Kluwer Academic Publishers: Dordrecht
    • (d) Organic Molecules for Nonlinear Optics and Photonics; Messier, J., Kajzar, F., Prasad, P., Eds.; Kluwer Academic Publishers: Dordrecht, 1991.
    • (1991) Organic Molecules for Nonlinear Optics and Photonics
  • 16
    • 0003423449 scopus 로고
    • Hann, R. A., Bloor, D., Eds.; Royal Society of Chemistry: London
    • (e) Organic Materials for Nonlinear Optics; Hann, R. A., Bloor, D., Eds.; Royal Society of Chemistry: London, 1989.
    • (1989) Organic Materials for Nonlinear Optics
  • 17
    • 33644522022 scopus 로고
    • (a) For a recent review of NLO studies involving organometallic and coordination complexes, see: Long, N. J. Angew. Chem., Int. Ed. Engl. 1995. 34, 21.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 21
    • Long, N.J.1
  • 18
    • 84990517353 scopus 로고
    • (b) For a review including early NLO studies, see: Nalwa, H. S. Appl. Organomet. Chem. 1991, 5, 349.
    • (1991) Appl. Organomet. Chem. , vol.5 , pp. 349
    • Nalwa, H.S.1
  • 19
    • 0001764117 scopus 로고    scopus 로고
    • For more recent NLO studies on organometallic and coordination complexes see, for example: (a) Cummings, S. D.; Cheng, L. T.; Eisenberg, R. Chem. Mater. 1997, 9, 440.
    • (1997) Chem. Mater. , vol.9 , pp. 440
    • Cummings, S.D.1    Cheng, L.T.2    Eisenberg, R.3
  • 29
    • 36749107537 scopus 로고
    • For a general discussion of the EFISH tecnique, see: (a) Oudar, J. L. J. Chem. Phys. 1977, 67, 446.
    • (1977) J. Chem. Phys. , vol.67 , pp. 446
    • Oudar, J.L.1
  • 32
    • 9844238004 scopus 로고    scopus 로고
    • note
    • 9c within a perturbation series expansion.
  • 39
    • 0003625968 scopus 로고
    • Wilkinson, G., Ed.; Pergamon Press: Oxford
    • Comprehensive Coordination Chemistry; Wilkinson, G., Ed.; Pergamon Press: Oxford, 1987; Vol. 2, p 730.
    • (1987) Comprehensive Coordination Chemistry , vol.2 , pp. 730
  • 40
    • 9844238561 scopus 로고    scopus 로고
    • note
    • Although a mixture of three stereoisomer s could in principle be formed in the condensation reaction to obtain ligands 4-6, the stereoisomer having both trans-imine linkages, i.e., with the enolimine tautomeric structure I in Scheme 1, is expected to be predominant. Moreover, since complexation involves only the dianion of stereoisomer I, no attempts to separate the mixture of the three stereoisomers were made.
  • 48
    • 9844257432 scopus 로고    scopus 로고
    • note
    • jjj)
  • 52
    • 9844221823 scopus 로고    scopus 로고
    • note
    • i components.
  • 53
    • 9844253745 scopus 로고    scopus 로고
    • note
    • ge and βμ values are computed because the ground- and excited-state dipole moments are both directed between the oxygen donor atoms.
  • 54
    • 9844264701 scopus 로고    scopus 로고
    • note
    • 27b
  • 64
    • 9844235197 scopus 로고    scopus 로고
    • note
    • 6a on 6a, an anti conformation was adopted, thus resulting in a slightly different calculated NLO response.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.