3,3′,5,5′-Tetranitrobiphenyl

被引:0
作者
Hammond, N. [1 ]
Carvalho, P. [1 ]
Wu, Y. [1 ]
Avery, M. A. [1 ,2 ,3 ]
机构
[1] Univ Mississippi, Dept Med Chem, University, MS 38677 USA
[2] Univ Mississippi, Sch Pharm, Pharmaceut Sci Res Inst, Natl Ctr Nat Prod Res, University, MS 38677 USA
[3] Univ Mississippi, Dept Chem & Biochem, University, MS 38677 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE | 2009年 / 65卷
基金
美国国家卫生研究院;
关键词
D O I
10.1107/S1600536809011088
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The title compound, C(12)H(6)N(4)O(8), is a biphenyl system that was synthesized as a building block for a new series of antimalarial compounds. The aromatic rings are oriented at a dihedral angle of 45.5 (2)degrees, and intermolecular short O center dot center dot center dot O contacts form a chain along the b axis. The strength of the interactions involved in this chain cause one of the rings to be slightly distorted, with the torsion angle between the nitro groups being 23.4 (2)degrees, whereas, in the other ring, both nitro systems are parallel, forming an angle of 9.6 (2)degrees with the plane of the aromatic ring to which they are bound. Furthermore, the three ring C atoms around the ring-ring linkage belong to a plane inclined by 4.5 (1)degrees in relation to the plane containing the other three C atoms, i.e. (NO(2)-)C-C-C(NO(2)). This distortion of the ring causes uncommonly short intermolecular O center dot center dot center dot O [3.038 (2) angstrom] and O center dot center dot center dot C [3.000 (4) and 3.214 (1) angstrom] contacts.
引用
收藏
页码:O1052 / U2301
页数:10
相关论文
共 50 条
  • [21] 3,3′,5,5′-Tetrabromo-4,4′-dihydroxybiphenyl
    Lehmler, HJ
    Parkin, S
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2005, 61 : O2828 - O2830
  • [22] CRYSTAL AND MOLECULAR-STRUCTURE OF 3,3',5,5'-TETRANITROBIPHENOL
    STARIKOVA, ZA
    SHCHEGOLEVA, TM
    TRUNOV, VK
    LANTRATOVA, OB
    POKROVSKAYA, IE
    JOURNAL OF STRUCTURAL CHEMISTRY, 1979, 20 (03) : 435 - 439
  • [23] Chloride analysis using 3,3',5,5'-tetramethylbenzidine and chloroperoxidase
    Keener, WK
    Watwood, ME
    ANALYTICAL BIOCHEMISTRY, 2004, 334 (02) : 406 - 408
  • [24] Biphenyl-3,3′,5,5′-tetracarboxylic acid
    Coles, SJ
    Holmes, R
    Hursthouse, MB
    Price, DJ
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2002, 58 : O626 - O628
  • [25] Two- and Three-Dimensional Polymeric Co(II) Terephthalates with 3,3′,5,5′-Tetrabromo-4,4′-bipyridine (3,3′5,5′-BrBipy)
    Sakhapov, I. F.
    Zagidullin, A. A.
    Islamov, D. R.
    Sharutin, V. V.
    Yakhvarov, D. G.
    Zherebtsov, D. A.
    Milyukov, V. A.
    Zaguzin, A. S.
    Fedin, V. P.
    Adonin, S. A.
    RUSSIAN JOURNAL OF COORDINATION CHEMISTRY, 2024, 50 (01) : 67 - 72
  • [26] SYNTHESIS AND MUTAGENICITY OF 3-HALOGENATED AND 3,3',5,5'-TETRAHALOGENATED BENZIDINES
    SAVARD, S
    JOSEPHY, PD
    MUTAGENESIS, 1987, 2 (02) : 97 - 99
  • [27] SURFACE-REACTIONS OF 3,3',5,5'-TETRAMETHYL BENZIDINE ON HECTORITE
    MCBRIDE, MB
    CLAYS AND CLAY MINERALS, 1985, 33 (06) : 510 - 516
  • [28] Tandem [5,5]-/[3,3]-Rearrangements of Aryl Sulfoxides with Allyl Nitriles
    Hu, Mengjie
    Ru, Liying
    Zhu, Mengjiao
    Yang, Shengwen
    Fan, Suojiang
    Ji, Jiangtao
    Zheng, Dingming
    Peng, Bo
    SYNTHESIS-STUTTGART, 2024, 56 (19): : 2973 - 2984
  • [29] Rationale of 3,3′,5,5′-Tetramethylbenzidine as the Chromogenic Substrate in Colorimetric Analysis
    Zhang, Xiao
    Yang, Qin
    Lang, Yunhe
    Jiang, Xia
    Wu, Peng
    ANALYTICAL CHEMISTRY, 2020, 92 (18) : 12400 - 12406
  • [30] Investigation of 3,3′,5,5′-tetramethylbenzidine as colorimetric substrate for a peroxidatic DNAzyme
    Li, Bingling
    Du, Yan
    Li, Tao
    Dong, Shaojun
    ANALYTICA CHIMICA ACTA, 2009, 651 (02) : 234 - 240