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Volumn 6, Issue 9, 2006, Pages 2007-2010

Solvent-dependent conformational switching of N-phenylhydroxamic acid and its application in crystal engineering

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Indexed keywords


EID: 33749018830     PISSN: 15287483     EISSN: None     Source Type: Journal    
DOI: 10.1021/cg060151z     Document Type: Article
Times cited : (36)

References (33)
  • 1
    • 0000527186 scopus 로고    scopus 로고
    • Irie, M., Ed.
    • (a) Irie, M., Ed. Chem. Rev. 2000, 100, 1683-1890.
    • (2000) Chem. Rev. , vol.100 , pp. 1683-1890
  • 11
    • 33749036145 scopus 로고    scopus 로고
    • note
    • In this paper, cis and trans are defined as shown in Figure 1 in order to describe the molecular conformations consistently, because E and Z can be interconverted simply by a change of the N-substituents.
  • 21
    • 33749005536 scopus 로고    scopus 로고
    • note
    • The concentration was 5 mg/mL for each experiment, and we confirmed that the concentration did not affect the ratio of the two conformers.
  • 22
    • 33749027917 scopus 로고    scopus 로고
    • note
    • 2 increased the ratio of the trans conformer to 59 and 69% (183 K), respectively.
  • 25
    • 0037165441 scopus 로고    scopus 로고
    • Recent examples of conformational polymorphism: (a) Yu, L. J. Phys. Chem. A 2002, 106, 544-550.
    • (2002) J. Phys. Chem. A , vol.106 , pp. 544-550
    • Yu, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.