Article
  • Intra-/Intermolecular Excimer Emission of Syndiotactic Polystyrene Having Carbazole Substituents
  • Jeong S, Jung IT, Yoon KB
  • 카바졸 치환체를 가지는 신디오탁틱 폴리스티렌의 분자내/분자간 엑시머 발광
  • 정선주, 정인태, 윤근병
Abstract
The syndiotactic and atactic poly(2-N-carbazoylmethyl)styrenes were obtained by a half-titanocene catalyst and a radical initiator for the investigation of photophysical properties, especially excimer formation. The atactic polymer exhibited only monomer emission, but the syndiotactic polymer showed both excimer emission and monomer emission resulting from the partial overlapping arrangement of carbazole pendants. The emission band of syndiotactic polymer was considerably dependent on solution concentration and temperature, however atactic polymer was independent because the excimer formation of syndiotactic helical conformation was more favorable than that of the random coil conformation of atactic polymer.

(2-N-carbazoylmethyl)styrene을 티타노센 촉매와 라디칼 개시제를 사용하여 신디오탁틱 및 아탁틱 poly (2-N-carbazoylmethyl)styrene을 합성하고 발광특성 중 엑시머 형성에 대하여 조사하였다. 어탁틱 고분자는 하나의 발광만을 나타낸 반면에 신디오탁틱 고분자는 카바졸기가 부분적으로 오버랩되는 정렬에서 기인하는 단량체 발광과 엑시머 발광을 모두 나타내었다. 아탁틱 고분자의 발광은 용액농도와 온도 의존성이 나타나지 않았으나, 신디오탁틱 고분자는 의존성의 크게 관찰되었다. 이러한 결과로 엑시머 발광은 치환기인 카바졸의 위치에 의존하는 것을 확인하였다.

Keywords: carbazole; polystyrene; tacticity; excimer; emission.

References
  • 1. Knolker HJ, Knoll J, Chem. Commun., 1170 (2003)
  •  
  • 2. Zhang Y, Cui Y, Prasad PN, Phys. Rev., B46, 9900 (1992)
  •  
  • 3. Scott JC, Pautmeier LT, Moerner WE, J. Opt. Soc. Am., B9, 2059 (1992)
  •  
  • 4. Tomas KRJ, Lin JT, Tao YT, Chuen CH, Chem. Mater., 14, 3852 (2002)
  •  
  • 5. Ostraskaite J, Voska V, Antulis J, Gaidelis V, Jankauskas V, Grazulevicius JV, J. Mater. Chem., 12, 3469 (2002)
  •  
  • 6. Romero DB, Nuesch F, Benazzi T, Ades D, Siove A, Zuppiroli L, Adv. Mater., 9(15), 1158 (1997)
  •  
  • 7. Grazulevicius JV, Strohriegl P, Pielichowski J, Pielichowski, Prog. Polym. Sci., 28, 1297 (2003)
  •  
  • 8. Chen YW, He YK, Wang F, Chen HY, Gong QH, Polymer, 42(3), 1101 (2001)
  •  
  • 9. Uryu T, Ohkawa H, Oshima R, Macromolecules., 20, 712 (1987)
  •  
  • 10. Sakai H, Itaya A, Masuhara H, Sasaki K, Kawata S, Polymer, 37(1), 31 (1996)
  •  
  • 11. de Sainte Claire P, J. Phys. Chem. B, 110(14), 7334 (2006)
  •  
  • 12. Itaya A, Okamoto K, Kusabayashi S, Bull. Chem. Soc. Jpn., 49, 2082 (1976)
  •  
  • 13. Evers F, Kobs K, Memming R, Terrell DR, J. Am.Chem. Soc., 105, 5988 (1983)
  •  
  • 14. Shimazu H, Kakinoya Y, Takehira K, Yoshihara T, Tobita S, Nakamura Y, Nishimura J, Bull. Chem. Soc. Jpn., 82, 860 (2009)
  •  
  • 15. Itoh Y, Nakada M, Sotoh H, Hachimori A, Webber SE, Macromolecules., 26, 1941 (1993)
  •  
  • 16. Klopffer W, Chem. Phys. Lett., 4, 193 (1969)
  •  
  • 17. Klopffer W, J. Chem. Phys., 50, 2337 (1969)
  •  
  • 18. Yeh KM, Lee CC, Chen Y, J. Polym. Sci. A: Polym. Chem., 46(15), 5180 (2008)
  •  
  • 19. Ishihara N, Seimiya T, Kuramoto M, Uoi M, Macromolecules., 19, 2464 (1986)
  •  
  • 20. Leibowitz M, Weinreb A, J. Chem. Phys., 46, 4652 (1967)
  •  
  • 21. Fox RB, Price TR, Cozzens RF, McDonald JR, J. Chem. Phys., 57, 534 (1972)
  •  
  • 22. Hoyle CE, Nemzek TL, Mar A, Guillet JE, Macromolecules., 11, 429 (1978)
  •  
  • 23. Yanari SS, Bovey FA, Lumry R, Nature., 200, 242 (1963)
  •  
  • 24. Frank CW, Harrah LA, J. Chem. Phys., 61, 1526 (1974)
  •  
  • 25. Longworth JW, Bovey FA, Biopolymers., 4, 1115 (1966)
  •  
  • 26. Longworth JW, Biopolymers., 4, 1131 (1966)
  •  
  • 27. Guerra G, Vitalino VM, De Rosa C, Petraccone V, Corradini P, Mcromolecules., 23, 1539 (1990)
  •  
  • 28. Albunia AR, Musto P, Guerra G, Polymer, 47(1), 234 (2006)
  •  
  • Polymer(Korea) 폴리머
  • Frequency : Bimonthly(odd)
    ISSN 0379-153X(Print)
    ISSN 2234-8077(Online)
    Abbr. Polym. Korea
  • 2023 Impact Factor : 0.4
  • Indexed in SCIE

This Article

  • 2011; 35(4): 314-319

    Published online Jul 25, 2011

  • Received on Jan 21, 2011
  • Accepted on Mar 30, 2011