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Volumn 14, Issue 1, 2012, Pages 138-146

Different crystal forms of a rich hydrogen bond acceptor compound resulting from alternative C-H⋯O and orthogonal CO⋯CO molecular interaction patterns

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EID: 82955165176     PISSN: None     EISSN: 14668033     Source Type: Journal    
DOI: 10.1039/c1ce05728f     Document Type: Article
Times cited : (9)

References (56)
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    • I. Y. H. Chan M. M. Bhadbhade R. Bishop Design of a new inclusion host: 3,7-diphenylbicyclo[3.3.0]octane- endo-3, endo-7-diol CrystEngComm 2011 13 3162
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    • The Shape Shifters
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  • 4
    • 84889407732 scopus 로고    scopus 로고
    • Nanoporous crystals, co-crystals, isomers and polymorphs from crystals
    • in, ed. J. L. Atwood and J. W. Steed, Wiley-VCH Verlag, Weinheim, 155-177
    • D. Braga, M. Curzi, S. L. Giaffreda, F. Grepioni, L. Maini, A. Pettersen and M. Polito, Nanoporous crystals, co-crystals, isomers and polymorphs from crystals, in Organic Nanostructures, ed., J. L. Atwood, and, J. W. Steed, Wiley-VCH Verlag, Weinheim, 2008, pp. 155-177
    • (2008) Organic Nanostructures
    • Braga, D.1    Curzi, M.2    Giaffreda, S.L.3    Grepioni, F.4    Maini, L.5    Pettersen, A.6    Polito, M.7
  • 12
    • 84954323241 scopus 로고    scopus 로고
    • Crystal Engineering of Pharmaceutical Co-Crystals
    • in, ed. E. R. T. Tiekink and J. J. Vittal, Wiley, Chichester, Ch. 2, pp 25-49
    • P. Vishweshwar, J. A. McMahon and M. J. Zaworotko, Crystal Engineering of Pharmaceutical Co-Crystals, in Frontiers in Crystal Engineering, ed., E. R. T. Tiekink, and, J. J. Vittal, Wiley, Chichester, 2006, Ch. 2, pp 25-49
    • (2006) Frontiers in Crystal Engineering
    • Vishweshwar, P.1    McMahon, J.A.2    Zaworotko, M.J.3
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    • Ph.D. Dissertation, The University of New South Wales, Sydney
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    • Djaidi, D.1
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    • Bruker Analytical X-ray Instruments Inc., Madison, WI, USA
    • APEX2 and SAINT, Bruker Analytical X-ray Instruments Inc., Madison, WI, USA, 2007
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.