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Volumn 46, Issue 22, 2007, Pages 4132-4135

A supramolecular approach to organic alloys: Cocrystals and three- and four-component solid solutions of 1,4-diazabicyclo[2.2.2]octane and 4-X-phenols (X = Cl, CH3, Br)

Author keywords

Crystal engineering; Organic alloys; Phenols; Solid solutions; Supramolecular chemistry

Indexed keywords

CRYSTAL ENGINEERING; CRYSTALLIZATION; PHENOLS; SOLID SOLUTIONS; SUBSTITUTION REACTIONS; SUPRAMOLECULAR CHEMISTRY;

EID: 34250765276     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200604830     Document Type: Article
Times cited : (78)

References (27)
  • 7
    • 34250745770 scopus 로고    scopus 로고
    • We do not consider solids with ionic components or solvates in which the component selection is largely circumstantial rather than by design
    • We do not consider solids with ionic components or solvates in which the component selection is largely circumstantial rather than by design.
  • 11
    • 0035801532 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 3240-3242;
    • (2001) Chem. Int. Ed , vol.40 , pp. 3240-3242
    • Angew1
  • 16
    • 33845204296 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 7546-7550.
    • (2006) Chem. Int. Ed , vol.45 , pp. 7546-7550
    • Angew1
  • 17
    • 34250749760 scopus 로고    scopus 로고
    • Solid solutions of metals or alloys are easy to form because of the spherical shape of the components and the isotropic nature of their intercomponent interactions
    • Solid solutions of metals or alloys are easy to form because of the spherical shape of the components and the isotropic nature of their intercomponent interactions.
  • 19
    • 27744451865 scopus 로고    scopus 로고
    • Note, however, that the multicomponent solid solutions in this work are based on ionic components
    • Angew. Chem. Int. Ed. 2005, 44, 7059-7062. Note, however, that the multicomponent solid solutions in this work are based on ionic components.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 7059-7062
  • 20
    • 0036022526 scopus 로고    scopus 로고
    • For example, solid solutions of insulin and a lipophilically modified insulin derivative show superior in vivo therapeutic properties; see: M. L. Brader, M. Sukumar, A. H. Pekar, D. S. McClellan, R. E. Chance, D. B. Flora, A. L. Cox, L. Irwin, S. R. Myers, Nat. Biotechnol. 2002, 20, 800-804. In this paper, homogeneous mixtures of insulin and its derivative are described as cocrystals. We note that these mixtures, though crystalline, are in fact members of a solid solution
    • For example, solid solutions of insulin and a lipophilically modified insulin derivative show superior in vivo therapeutic properties; see: M. L. Brader, M. Sukumar, A. H. Pekar, D. S. McClellan, R. E. Chance, D. B. Flora, A. L. Cox, L. Irwin, S. R. Myers, Nat. Biotechnol. 2002, 20, 800-804. In this paper, homogeneous mixtures of insulin and its derivative are described as cocrystals. We note that these mixtures, though crystalline, are in fact members of a solid solution.
  • 22
    • 34250727090 scopus 로고    scopus 로고
    • In contrast, the repeat units in traditional solid solutions of organic compounds are single molecules, for example, anthracene and acridine see ref, 3] for more examples
    • In contrast, the repeat units in traditional solid solutions of organic compounds are single molecules, for example, anthracene and acridine (see ref. [3] for more examples).
  • 23
    • 34250699516 scopus 로고    scopus 로고
    • Single-crystal X-ray diffraction data were collected on a Bruker SMART CCD diffractometer using MoKα radiation. All the structures were solved by direct methods and refined on F2 by least-squares methods using the program SHELXL-97. Crystal data for ClCl: C18H22Cl2N2O2, Mr, 369.28, monoclinic, a, 17.987(5, b, 9.256(2, c, 11.241(3) Å, β, 101.848(4)°, V, 1831.7(8) Å3, T, 193K, space group C2/c (no. 15, Z, 4, ρcalcd, 1-339 g cm-3, μ(MoKα, 0.367 mm-1, 1739 reflections of 2138 unique reflections with I >2σI, 2.31 < θ < 27.86°, R1, 0.045, wR2, 0.125. Crystal data for MeMe: C20H28N2O2, Mr
    • 2 = 0.114. ClMeBr: Only cell parameters are reported herein (Table 1); a full structural analysis will be published elsewhere. CCDC-628798 (ClCl), CCDC-628799 (MeMe), CCDC-628800 (BrBr), CCDC-628801 (ClMe), CCDC-628802 (ClBr), and CCDC-628803 (MeBr) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 24
    • 34250736847 scopus 로고    scopus 로고
    • The crystal structure of MeMe was previously determined at 295 K; see: M. Takama, M. Yasui, S. Harada, N. Kasai, K. Tanaka, F. Toda, Bull. Chem. Soc. Jpn. 1988, 61, 567-568.
    • The crystal structure of MeMe was previously determined at 295 K; see: M. Takama, M. Yasui, S. Harada, N. Kasai, K. Tanaka, F. Toda, Bull. Chem. Soc. Jpn. 1988, 61, 567-568.
  • 25
    • 37049079749 scopus 로고    scopus 로고
    • Type-I contact: Br⋯Br 3.658 Å, C-Br⋯Br 158.0°; type-II contact: Br⋯Br 3.632 Å, C-Br⋯Br 160.5, 119.1°; V. R. Pedireddi, D. S. Reddy, B. S. Goud, D. C. Craig, A. D. Rae, G. R. Desiraju, J. Chem. Soc. Perkin Trans. 2 1994, 2353-2360.
    • Type-I contact: Br⋯Br 3.658 Å, C-Br⋯Br 158.0°; type-II contact: Br⋯Br 3.632 Å, C-Br⋯Br 160.5, 119.1°; V. R. Pedireddi, D. S. Reddy, B. S. Goud, D. C. Craig, A. D. Rae, G. R. Desiraju, J. Chem. Soc. Perkin Trans. 2 1994, 2353-2360.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.