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Volumn 7, Issue , 2005, Pages 439-448

Building co-crystals with molecular sense and supramolecular sensibility

Author keywords

[No Author keywords available]

Indexed keywords


EID: 25844449757     PISSN: 14668033     EISSN: None     Source Type: Journal    
DOI: 10.1039/b505883j     Document Type: Review
Times cited : (716)

References (130)
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    • J.-M. Lehn, Science, 2002, 295, 2400;
    • (2002) Science , vol.295 , pp. 2400
    • Lehn, J.-M.1
  • 20
    • 25844460596 scopus 로고    scopus 로고
    • note
    • A solid containing building blocks with formal charges is a salt, and there is no need to describe it as an adduct, molecular adduct, proton-transfer solid, molecular salt, or variations hereof.
  • 21
    • 0037878053 scopus 로고    scopus 로고
    • One could also make a case for including materials such as those prepared through co-condensation at reduced temperatures or elevated pressure in very elegant ways by Boese and co-workers: R. Boese, M. T. Kirchner, W. E. Billups and L. R. Norman, Angew. Chem. Int. Ed., 2003, 42, 1961.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 1961
    • Boese, R.1    Kirchner, M.T.2    Billups, W.E.3    Norman, L.R.4
  • 22
    • 25844526588 scopus 로고    scopus 로고
    • note
    • Other intermolecular forces such as py⋯iodo will also be included.
  • 75
    • 3242763358 scopus 로고    scopus 로고
    • The crystal structure of tetrafluoro-1,4-diiodobenzene tetramethyl-1,4-dicyanobenzene represents a rare example of a co-crystal assembled via CN⋯I interactions: D. Britton and W. B. Gleason, Acta Crystallogr., Sect. E, 2002, 58, o1375.
    • (2002) Acta Crystallogr., Sect. E , vol.58
    • Britton, D.1    Gleason, W.B.2
  • 76
    • 0142042391 scopus 로고    scopus 로고
    • There are, however, examples of co-crystals formed between 1,2-dibromotetrafluoroethane and N-heterocycles such a 1,4-dimethylpiperazine: Q. Chu, Z. Wang, Q. Huang, C. Yan and S. Zhu, New. J. Chem., 2003, 27, 1522.
    • (2003) New. J. Chem. , vol.27 , pp. 1522
    • Chu, Q.1    Wang, Z.2    Huang, Q.3    Yan, C.4    Zhu, S.5
  • 86
    • 25844518704 scopus 로고    scopus 로고
    • CSD codes: OCAYUM, OCASAT, and POFPAB
    • CSD codes: OCAYUM, OCASAT, and POFPAB.
  • 87
    • 25844438433 scopus 로고    scopus 로고
    • CSD codes: GURVOE, GURVUK, LUDFUL, UNECAR, ZUPKUQ, and ZUPLAX
    • CSD codes: GURVOE, GURVUK, LUDFUL, UNECAR, ZUPKUQ, and ZUPLAX.
  • 88
    • 25844468566 scopus 로고    scopus 로고
    • CSD codes: BEQWAV, FIHYEA, FIJCIK, FIJCUW, HUPPOX, MUFNIK, NOPXIZ, OJENIA, PULWUO, RAPHAR, SUXVOW, UDUZIC, UDOZOI, UHELUO, XUNGIW, and XUNGOC
    • CSD codes: BEQWAV, FIHYEA, FIJCIK, FIJCUW, HUPPOX, MUFNIK, NOPXIZ, OJENIA, PULWUO, RAPHAR, SUXVOW, UDUZIC, UDOZOI, UHELUO, XUNGIW, and XUNGOC.
  • 89
    • 25844484783 scopus 로고    scopus 로고
    • CSD code: POFPEF
    • CSD code: POFPEF.
  • 90
    • 25844513672 scopus 로고    scopus 로고
    • CSD codes: CUFSET, LUSWEB, PANYIM, PANZEJ, PAPDIT, PAPFOB, UNEBOE, WUKREZ, and WUKROJ
    • CSD codes: CUFSET, LUSWEB, PANYIM, PANZEJ, PAPDIT, PAPFOB, UNEBOE, WUKREZ, and WUKROJ.
  • 91
    • 25844502571 scopus 로고    scopus 로고
    • CSD codes: AJAKEB, AJAKIF, ASAXOH, ASAXUN, BUDWEC, BUDZUV, BUFBIP, BUFQAU, LUNMEM, LUNMIC, LUNMOW, and VAKTOR
    • CSD codes: AJAKEB, AJAKIF, ASAXOH, ASAXUN, BUDWEC, BUDZUV, BUFBIP, BUFQAU, LUNMEM, LUNMIC, LUNMOW, and VAKTOR.
  • 95
    • 25844484143 scopus 로고    scopus 로고
    • note
    • There are, of course, other aspects that need to be considered e.g., solubility differences between drug and CA (if the co-crystals are to be prepared via solution-based methods) before embarking upon a series of co-crystallizations.
  • 113
    • 0031780159 scopus 로고    scopus 로고
    • If the acid is too strong, the proton will be transferred to the nitrogen atom resulting in an ionic compound and not a co-crystal. Some examples of crystal engineering of ionic systems include e.g.: J. A. Swift, A. M. Pivovar, A. M. Reynolds and M. D. Ward, J. Am. Chem. Soc., 1998, 120, 5887;
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5887
    • Swift, J.A.1    Pivovar, A.M.2    Reynolds, A.M.3    Ward, M.D.4
  • 126
    • 25844482652 scopus 로고    scopus 로고
    • note
    • a = 4.72 ± 0.10 and 5.85 ± 0.18 for pyridyl and benzimidazol-1-yl moieties, respectively. The calculations were performed using Advanced Chemistry Development (ACD/Labs) Software Solaris V4.76 (© 1994-2005 ACD/Labs).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.