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Volumn 129, Issue 21, 2007, Pages 6688-6689

Chiral amplification of chiral porphyrin derivatives by templated heteroaggregation

Author keywords

[No Author keywords available]

Indexed keywords

PORPHYRIN DERIVATIVE;

EID: 34249781693     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja071249k     Document Type: Article
Times cited : (53)

References (27)
  • 7
    • 0037266843 scopus 로고    scopus 로고
    • and references therein
    • Pasternack, R. F. Chirality, 2003, 15, 329, and references therein.
    • (2003) Chirality , vol.15 , pp. 329
    • Pasternack, R.F.1
  • 19
    • 34249809790 scopus 로고    scopus 로고
    • 2O/EtOH (v/v) final solvent composition.
    • 2O/EtOH (v/v) final solvent composition.
  • 20
    • 34249780885 scopus 로고    scopus 로고
    • 2 (≥30 μM). However, this is accompanied by evident cloudiness of the solutions, with consequent precipitation of some solid material occurring with time.
    • 2 (≥30 μM). However, this is accompanied by evident cloudiness of the solutions, with consequent precipitation of some solid material occurring with time.
  • 23
    • 34249774947 scopus 로고    scopus 로고
    • 2 (425 nm) aggregates indicate negligible electronic coupling between porphyrin heteroaggregates.
    • 2 (425 nm) aggregates indicate negligible electronic coupling between porphyrin heteroaggregates.
  • 24
    • 0037051625 scopus 로고    scopus 로고
    • The kinetic rate constant values obtained by CD spectroscopy are somewhat higher than those calculated by UV-visible, spectroscopy. This is commonly observed in templated aggregation of water-soluble porphyrin derivatives on DNA matrices, a Pasternack, R. F, Gibbs, E. J, Bruzewicz, D, Stewart, D, Shannon, K. Engstrom, J. Am. Chem. Soc. 2002, 124, 3533
    • The kinetic rate constant values obtained by CD spectroscopy are somewhat higher than those calculated by UV-visible, spectroscopy. This is commonly observed in templated aggregation of water-soluble porphyrin derivatives on DNA matrices. (a) Pasternack, R. F.; Gibbs, E. J.; Bruzewicz, D.; Stewart, D.; Shannon, K. Engstrom, J. Am. Chem. Soc. 2002, 124, 3533.
  • 26
    • 2442584691 scopus 로고    scopus 로고
    • These results can be of importance for the exploitation of the phenomena involved in the hierarchical heteroassembly of porphyrin derivatives. See for example De Napoli, M, Nardis, S, Paolesse, R, Vicente, M. G. H, Lauceri, R, Purrello, R. J. Am. Chem. Soc. 2004, 126, 5934
    • These results can be of importance for the exploitation of the phenomena involved in the hierarchical heteroassembly of porphyrin derivatives. See for example De Napoli, M.; Nardis, S.; Paolesse, R.; Vicente, M. G. H.; Lauceri, R.; Purrello, R. J. Am. Chem. Soc. 2004, 126, 5934.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.