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Volumn 31, Issue 14, 1998, Pages 4666-4668

Temperature dependent CD spectra of poly(dihexylsilylene)s with terminal chiral groups. Coupled cotton effects of silicon σ chains

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION SPECTROSCOPY; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STRUCTURE (COMPOSITION); SYNTHESIS (CHEMICAL); ULTRAVIOLET SPECTROSCOPY;

EID: 0032121209     PISSN: 00249297     EISSN: None     Source Type: Journal    
DOI: 10.1021/ma980427e     Document Type: Article
Times cited : (40)

References (29)
  • 1
    • 0024733839 scopus 로고
    • For reviews, see: (a) Miller, R. D.; Michl, J. Chem. Rev. 1989, 89, 1359. (b) Michl, J.; Downing, J. W.; Karatsu, T.; McKinley, A. J.; Poggi, G.; Wallraff, G. M.; Sooriyakumaran, R.; Miller, R. D. Pure Appl. Chem. 1988, 60, 959. (c) Zeigler, J. M. Synth. Met. 1989, 28, C581. (d) West, R. J. Organomet. Chem. 1986, 300, 327. (d) West, R. In The Chemistry of Organosilicon Compounds; Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, England, 1989; Chapter 19, p 1207.
    • (1989) Chem. Rev. , vol.89 , pp. 1359
    • Miller, R.D.1    Michl, J.2
  • 2
    • 84941838211 scopus 로고
    • For reviews, see: (a) Miller, R. D.; Michl, J. Chem. Rev. 1989, 89, 1359. (b) Michl, J.; Downing, J. W.; Karatsu, T.; McKinley, A. J.; Poggi, G.; Wallraff, G. M.; Sooriyakumaran, R.; Miller, R. D. Pure Appl. Chem. 1988, 60, 959. (c) Zeigler, J. M. Synth. Met. 1989, 28, C581. (d) West, R. J. Organomet. Chem. 1986, 300, 327. (d) West, R. In The Chemistry of Organosilicon Compounds; Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, England, 1989; Chapter 19, p 1207.
    • (1988) Pure Appl. Chem. , vol.60 , pp. 959
    • Michl, J.1    Downing, J.W.2    Karatsu, T.3    McKinley, A.J.4    Poggi, G.5    Wallraff, G.M.6    Sooriyakumaran, R.7    Miller, R.D.8
  • 3
    • 0024301213 scopus 로고
    • For reviews, see: (a) Miller, R. D.; Michl, J. Chem. Rev. 1989, 89, 1359. (b) Michl, J.; Downing, J. W.; Karatsu, T.; McKinley, A. J.; Poggi, G.; Wallraff, G. M.; Sooriyakumaran, R.; Miller, R. D. Pure Appl. Chem. 1988, 60, 959. (c) Zeigler, J. M. Synth. Met. 1989, 28, C581. (d) West, R. J. Organomet. Chem. 1986, 300, 327. (d) West, R. In The Chemistry of Organosilicon Compounds; Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, England, 1989; Chapter 19, p 1207.
    • (1989) Synth. Met. , vol.28
    • Zeigler, J.M.1
  • 4
    • 0001060404 scopus 로고
    • For reviews, see: (a) Miller, R. D.; Michl, J. Chem. Rev. 1989, 89, 1359. (b) Michl, J.; Downing, J. W.; Karatsu, T.; McKinley, A. J.; Poggi, G.; Wallraff, G. M.; Sooriyakumaran, R.; Miller, R. D. Pure Appl. Chem. 1988, 60, 959. (c) Zeigler, J. M. Synth. Met. 1989, 28, C581. (d) West, R. J. Organomet. Chem. 1986, 300, 327. (d) West, R. In The Chemistry of Organosilicon Compounds; Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, England, 1989; Chapter 19, p 1207.
    • (1986) J. Organomet. Chem. , vol.300 , pp. 327
    • West, R.1
  • 5
    • 0001269445 scopus 로고
    • Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, England, Chapter 19
    • For reviews, see: (a) Miller, R. D.; Michl, J. Chem. Rev. 1989, 89, 1359. (b) Michl, J.; Downing, J. W.; Karatsu, T.; McKinley, A. J.; Poggi, G.; Wallraff, G. M.; Sooriyakumaran, R.; Miller, R. D. Pure Appl. Chem. 1988, 60, 959. (c) Zeigler, J. M. Synth. Met. 1989, 28, C581. (d) West, R. J. Organomet. Chem. 1986, 300, 327. (d) West, R. In The Chemistry of Organosilicon Compounds; Patai, S., Rappoport, Z., Eds.; J. Wiley and Sons: Chichester, England, 1989; Chapter 19, p 1207.
    • (1989) The Chemistry of Organosilicon Compounds , pp. 1207
    • West, R.1
  • 11
    • 85034471592 scopus 로고    scopus 로고
    • note
    • 22D = -14.5 (c 10.0, cyclohexane).
  • 12
    • 85034479291 scopus 로고    scopus 로고
    • note
    • w = 12000. The percent incorporation of the terminal chiral group in a polymer was calculated to be 18% for 1a and 1b based on the relative intensity of the hexyl α-methylene + methyl protons with that of phenyl protons.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.