메뉴 건너뛰기




Volumn 46, Issue 17, 2007, Pages 3033-3036

Triangle-shaped polycyclic aromatic hydrocarbons

Author keywords

Helical structures; Liquid crystals; Polycycles; Scanning probe microscopy; Self assembly

Indexed keywords

MOLECULAR STRUCTURE; SCANNING PROBE MICROSCOPY; SELF ASSEMBLY; SYNTHESIS (CHEMICAL); THERMAL EFFECTS;

EID: 34250846466     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200605224     Document Type: Article
Times cited : (124)

References (42)
  • 8
    • 24944516927 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5592-5629.
    • (2005) Chem. Int. Ed , vol.44 , pp. 5592-5629
    • Angew1
  • 12
    • 1042268165 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 755-758.
    • (2004) Chem. Int. Ed , vol.43 , pp. 755-758
    • Angew1
  • 18
    • 0034302780 scopus 로고    scopus 로고
    • See Supporting Information for the spectra, and: L. Przybilla, J. D. Brand, K. Yoshimura, J. Räder, K. Müllen, Anal. Chem. 2000, 72, 4591-4597.
    • See Supporting Information for the spectra, and: L. Przybilla, J. D. Brand, K. Yoshimura, J. Räder, K. Müllen, Anal. Chem. 2000, 72, 4591-4597.
  • 19
    • 34250837146 scopus 로고    scopus 로고
    • The detection of the α band is difficult because of the extremely low intensity of this band. However, the β band at 400 nm and the p band as the shoulder at 450 nm are clearly resolved and show significant bathochromic shifts compared to the parent HBC (β band at 359 nm).
    • The detection of the α band is difficult because of the extremely low intensity of this band. However, the β band at 400 nm and the p band as the shoulder at 450 nm are clearly resolved and show significant bathochromic shifts compared to the parent HBC (β band at 359 nm).
  • 20
    • 34250901218 scopus 로고    scopus 로고
    • More details of calculations can be found in the Supporting Information
    • More details of calculations can be found in the Supporting Information.
  • 21
    • 34250813370 scopus 로고    scopus 로고
    • PhD thesis, Mainz University
    • C. Simpson, PhD thesis, Mainz University, 2006.
    • (2006)
    • Simpson, C.1
  • 22
    • 0344666656 scopus 로고    scopus 로고
    • This was probably because the sulfur atoms in fused oligothiophene rings did not improve conjugation, but instead led to a nonplanar molecular conformation (see also the 6-31G** calculations in the Supporting Information, a) X. Zhang, A. J. Matzger, J. Org. Chem. 2003, 68, 9813-9815;
    • This was probably because the sulfur atoms in fused oligothiophene rings did not improve conjugation, but instead led to a nonplanar molecular conformation (see also the 6-31G** calculations in the Supporting Information), a) X. Zhang, A. J. Matzger, J. Org. Chem. 2003, 68, 9813-9815;
  • 28
    • 0344875948 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 5329-5333;
    • (2003) Chem. Int. Ed , vol.42 , pp. 5329-5333
    • Angew1
  • 32
    • 31444442257 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 819-823.
    • (2006) Chem. Int. Ed , vol.45 , pp. 819-823
    • Angew1
  • 36
    • 34250885975 scopus 로고    scopus 로고
    • 2.
    • 2.
  • 37
    • 0036432919 scopus 로고    scopus 로고
    • Hydrogen-bonding-induced honeycomb: a Y. Ishikawa, A. Ohira, M. Sakata, C. Hirayama, M. Kunitake, Chem. Commun. 2002, 2652-2653;
    • Hydrogen-bonding-induced honeycomb: a) Y. Ishikawa, A. Ohira, M. Sakata, C. Hirayama, M. Kunitake, Chem. Commun. 2002, 2652-2653;
  • 40
    • 33645411648 scopus 로고    scopus 로고
    • van der Waals interaction induced honeycomb: d S. Furukawa, H. Uji-I, K. Tahara, T. Ichikawa, M. Sonoda, F. C. De Schryver, Y. Tobe, S. De Feyter, J. Am. Chem. Soc. 2006, 128, 3502-3503.
    • van der Waals interaction induced honeycomb: d) S. Furukawa, H. Uji-I, K. Tahara, T. Ichikawa, M. Sonoda, F. C. De Schryver, Y. Tobe, S. De Feyter, J. Am. Chem. Soc. 2006, 128, 3502-3503.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.