메뉴 건너뛰기




Volumn 11, Issue 4, 2011, Pages 972-981

Effect of fluorination on molecular conformation in the solid state: Tuning the conformation of cocrystal formers

Author keywords

[No Author keywords available]

Indexed keywords

ACID DISSOCIATION; ADIPIC ACIDS; CAMBRIDGE; CO-CRYSTALS; COMPUTATIONAL ANALYSIS; CONFORMATIONAL ANALYSIS; CONFORMATIONAL BEHAVIOR; CONFORMATIONAL PREFERENCES; CONFORMATIONAL PROPERTIES; CRYSTAL STRUCTURE ANALYSIS; CRYSTAL STRUCTURE DETERMINATION; DATABASE ANALYSIS; METAL-ORGANIC; MOLECULAR BUILDING BLOCKS; MOLECULAR CONFORMATION; MOLECULAR SHAPES; MOLECULAR SIZE; MULTICOMPONENTS; NEUTRAL MOLECULES; PERFLUOROCARBONS; PHARMACEUTICAL INGREDIENTS; RESULTING MATERIALS; SINGLE MOLECULE; SOLID-STATE STRUCTURES; SOLUTION NMR; STATE BEHAVIOR;

EID: 79953873122     PISSN: 15287483     EISSN: 15287505     Source Type: Journal    
DOI: 10.1021/cg1016388     Document Type: Article
Times cited : (19)

References (78)
  • 23
    • 79953853050 scopus 로고    scopus 로고
    • Eddaoudi, M.; Moler, D. B.; Li, H.; Chen, B.; Reineke, T. M.; OKeeffe, M.; Yaghi, O. M.
    • Eddaoudi, M.; Moler, D. B.; Li, H.; Chen, B.; Reineke, T. M.; OKeeffe, M.; Yaghi, O. M.
  • 40
    • 61649110742 scopus 로고    scopus 로고
    • Fluorinated iodo- and bromo-benzoic acids and oximes capable of simultaneous hydrogen- and halogen-bonding have recently been used in cocrystal synthesis, see
    • Fluorinated iodo- and bromo-benzoic acids and oximes capable of simultaneous hydrogen- and halogen-bonding have recently been used in cocrystal synthesis, see Aakeröy, C. B.; Schultheiss, N. C.; Rajbanshi, A.; Desper, J.; Moore, C. Cryst Growth Des. 2009, 9, 432-441
    • (2009) Cryst Growth Des. , vol.9 , pp. 432-441
    • Aakeröy, C.B.1    Schultheiss, N.C.2    Rajbanshi, A.3    Desper, J.4    Moore, C.5
  • 44
    • 33645039124 scopus 로고    scopus 로고
    • Increasing coformer acidity aids cocrystallisation
    • Increasing coformer acidity aids cocrystallisation: Aakeröy, C. B.; Desper, J.; Scott, B. M. T. Chem. Commun. 2006, 1445-1447
    • (2006) Chem. Commun. , pp. 1445-1447
    • Aakeröy, C.B.1    Desper, J.2    Scott, B.M.T.3
  • 57
    • 79953865511 scopus 로고    scopus 로고
    • The decorated chain motif in previously reported (caf)·(L-tartaric acid) (26) does not increase the acidity of carboxylic acids bonded to caf, as the chains are held by O-H⋯O bonds between carboxylic acid donors and alcohol acceptors.
    • The decorated chain motif in previously reported (caf)·(L-tartaric acid) (26) does not increase the acidity of carboxylic acids bonded to caf, as the chains are held by O-H⋯O bonds between carboxylic acid donors and alcohol acceptors.
  • 61
    • 34447524850 scopus 로고    scopus 로고
    • For examples of using solid-state NMR to differentiate between cocrystals, salts and polymorphs, see
    • For examples of using solid-state NMR to differentiate between cocrystals, salts and polymorphs, see Burley, J. C.; Duer, M. J.; Stein, R. S.; Vrcelj, R. M. Eur. J. Pharm. Sci. 2007, 31, 271-276
    • (2007) Eur. J. Pharm. Sci. , vol.31 , pp. 271-276
    • Burley, J.C.1    Duer, M.J.2    Stein, R.S.3    Vrcelj, R.M.4
  • 70
    • 41149161115 scopus 로고    scopus 로고
    • The opposite effect, where the crystal structure enforces an unfavourable molecular conformation was recently described
    • The opposite effect, where the crystal structure enforces an unfavourable molecular conformation was recently described: Friščić, T.; Fábián, L.; Burley, J. C.; Reid, D. G.; Duer, M. J.; Jones, W. Chem. Commun. 2008, 1644-1646
    • (2008) Chem. Commun. , pp. 1644-1646
    • Friščić, T.1    Fábián, L.2    Burley, J.C.3    Reid, D.G.4    Duer, M.J.5    Jones, W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.