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7
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34250745770
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We do not consider solids with ionic components or solvates in which the component selection is largely circumstantial rather than by design
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We do not consider solids with ionic components or solvates in which the component selection is largely circumstantial rather than by design.
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8
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33645281070
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D. E. Lynch, G. Smith, K. A. Byriel, C. H. L. Kennard, J. Chem. Soc. Chem. Commun. 1992, 300-301;
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Lynch, D.E.1
Smith, G.2
Byriel, K.A.3
Kennard, C.H.L.4
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9
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0003934264
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T. Smolka, R. Boese, R. Sustmann, Struct. Chem. 1999, 10, 429-431;
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Smolka, T.1
Boese, R.2
Sustmann, R.3
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10
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4243780319
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C. B. Aakeröy, A. M. Beatty, B. A. Helfrich, Angew. Chem. 2001, 113, 3340-3342;
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Angew. Chem
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, pp. 3340-3342
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Aakeröy, C.B.1
Beatty, A.M.2
Helfrich, B.A.3
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11
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0035801532
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Angew. Chem. Int. Ed. 2001, 40, 3240-3242;
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(2001)
Chem. Int. Ed
, vol.40
, pp. 3240-3242
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Angew1
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12
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0344861922
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E. Y. Cheung, S. J. Kitchin, K. D. M. Harris, Y. Imai, N. Tajima, R. Kuroda, J. Am. Chem. Soc. 2003, 125, 14658-14659;
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J. Am. Chem. Soc
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Cheung, E.Y.1
Kitchin, S.J.2
Harris, K.D.M.3
Imai, Y.4
Tajima, N.5
Kuroda, R.6
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14
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25444484704
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B. R. Bhogala, S. Basavoju, A. Nangia, Cryst. Growth Des. 2005, 5, 1683-1686;
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(2005)
Cryst. Growth Des
, vol.5
, pp. 1683-1686
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Bhogala, B.R.1
Basavoju, S.2
Nangia, A.3
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15
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34250720041
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T. Friščić, A. V. Trask, W. Jones, W. D. S. Motherwell, Angew. Chem. 2006, 118, 7708-7712;
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(2006)
Angew. Chem
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Friščić, T.1
Trask, A.V.2
Jones, W.3
Motherwell, W.D.S.4
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16
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33845204296
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Angew. Chem. Int. Ed. 2006, 45, 7546-7550.
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(2006)
Chem. Int. Ed
, vol.45
, pp. 7546-7550
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Angew1
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34250749760
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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
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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.
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18
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33746272516
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For an exception, see
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For an exception, see: K. Sada, K. Inoue, T. Tanaka, A. Epergyes, A. Tanaka, N. Tohnai, A. Matsumoto, M. Miyata, Angew. Chem. 2005, 117, 7221-7224;
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(2005)
Angew. Chem
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, pp. 7221-7224
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Sada, K.1
Inoue, K.2
Tanaka, T.3
Epergyes, A.4
Tanaka, A.5
Tohnai, N.6
Matsumoto, A.7
Miyata, M.8
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19
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27744451865
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Note, however, that the multicomponent solid solutions in this work are based on ionic components
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Angew. Chem. Int. Ed. 2005, 44, 7059-7062. Note, however, that the multicomponent solid solutions in this work are based on ionic components.
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(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 7059-7062
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20
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0036022526
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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
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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.
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22
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34250727090
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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
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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).
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23
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34250699516
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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.
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24
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34250736847
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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.
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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.
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25
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37049079749
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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.
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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.
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A. V. Trask, W. D. S. Motherwell, W. Jones, Cryst. Growth Des. 2005, 5, 1013-1021.
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(2005)
Cryst. Growth Des
, vol.5
, pp. 1013-1021
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Trask, A.V.1
Motherwell, W.D.S.2
Jones, W.3
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