Polymorphs and pseudopolymorphs of N,N′-dithiobisphthalimide

被引:14
作者
Farrell, DMM
Glidewell, C [1 ]
Low, JN
Skakle, JMS
Zakaria, CM
机构
[1] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Dundee, Sch Engn, Dundee DD1 4HN, Scotland
[3] Univ Aberdeen, Dept Chem, Aberdeen AB9 1FX, Scotland
关键词
D O I
10.1107/S0108768101020006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
N,N'-Dithiobisphthalimide, C16H8N2O4S2 (I), forms a wide range of polymorphs and solvates (pseudopolymorphs). When (I) is crystallized from methanol it yields a solvent-free polymorph (4), in Pna2(1) with Z' = 1, in which the molecules are linked into chains by a single C-H...O hydrogen bond: crystallization from either acetonitrile or dimethylformamide produces a monoclinic polymorph (5), in P2(1)/c with Z' = 2, also solvent-free, in which the molecules are linked into molecular ladders. Nitromethane forms a monosolvate, C16H8N2O4S2.CH3NO2 (6), in P2(1)/c with Z' = 1, in which the solvent molecules are linked to the molecules of (I) not only via a conventional C-H...O hydrogen bond but also via a polarized multicentre interaction involving all three C-H bonds of the solvent molecule. Chlorobenzene forms a precise hemisolvate, C16H8N2O4S2.0.5C(6)H(5)Cl (7), in P (1) over bar with Z' = 1, while ethylbenzene forms an approximate hemisolvate 2C(16)H(8)N(2)O(4)S(2).0.913C(6)H(5)C(2)H(5).0.087H(2)O (8), in P2(1)/c with eight molecules of (I) per unit cell. In both solvates the molecules of (I) are linked, in (7) by pi...pi stacking interactions augmented by weak C-H...O hydrogen bonds and in (8) by stronger C-H...O hydrogen bonds: the solvent molecules lie in isolated cavities, disordered across inversion centres in (7) and fully ordered in general positions in (8). Crystallization of (I) either from tetrahydrofuran or from wet tert-butanol yields isomorphous solvates (9) and (10), respectively, in C2/c with Z' = 0.5, in which molecules of (I) lie across twofold rotation axes and are linked by pi...pi stacking interactions and very weak C-H...O hydrogen bonds, forming a framework enclosing continuous channels: highly disordered solvent molecules lie within these channels. p-Xylene and toluene form isomorphous hemisolvates (11) and (12) with unit cells metrically very similar to those of (9) and (10), but in P2(1)/n with Z' = 1: in these two solvates the molecules of (I) are linked into a framework by very short C-H...O hydrogen bonds; the solvent molecules lie within continuous channels, but they are localized across inversion centres so that the toluene is disordered across an inversion centre.
引用
收藏
页码:289 / 299
页数:11
相关论文
共 17 条
  • [1] Allen F.H., 1993, CHEM AUTOMAT NEWS, V8, P31
  • [2] Over one hundred solvates of sulfathiazole
    Bingham, AL
    Hughes, DS
    Hursthouse, MB
    Lancaster, RW
    Tavener, S
    Threlfall, TL
    [J]. CHEMICAL COMMUNICATIONS, 2001, (07) : 603 - 604
  • [3] Chiral versus racemic building blocks in supramolecular chemistry:: tartrate salts of organic diamines
    Farrell, DMM
    Ferguson, G
    Lough, AJ
    Glidewell, C
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2002, 58 (02) : 272 - 288
  • [4] FERGUSON G, 1999, PRPKAPPA
  • [5] Reporting and evaluating absolute-structure and absolute-configuration determinations
    Flack, HD
    Bernardinelli, G
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2000, 33 : 1143 - 1148
  • [6] ON ENANTIOMORPH-POLARITY ESTIMATION
    FLACK, HD
    [J]. ACTA CRYSTALLOGRAPHICA SECTION A, 1983, 39 (NOV): : 876 - 881
  • [7] Polymorphs and pseudo-polymorphs of μ-oxo-bis{[N,N′-bis(salicylidene)propane-1,3-diamine]oxorhenium(V)}
    Kooijman, H
    van Bommel, KJC
    Verboom, W
    Reinhoudt, DN
    Kroon, J
    Spek, AL
    [J]. ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 2000, 56 : 749 - 757
  • [8] A test of crystal structure prediction of small organic molecules
    Lommerse, JPM
    Motherwell, WDS
    Ammon, HL
    Dunitz, JD
    Gavezzotti, A
    Hofmann, DWM
    Leusen, FJJ
    Mooij, WTM
    Price, SL
    Schweizer, B
    Schmidt, MU
    van Eijck, BP
    Verwer, P
    Williams, DE
    [J]. ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2000, 56 (04) : 697 - 714
  • [9] Pseudopolymorphism: occurrences of hydrogen bonding organic solvents in molecular crystals
    Nangia, A
    Desiraju, GR
    [J]. CHEMICAL COMMUNICATIONS, 1999, (07) : 605 - 606
  • [10] *NON BV, 1997, KAPP CCD SERV SOFTW