Crystal structure of (+/-)-1-({[4-(allyloxy)phenyl]sulfanyl}methyl)-2-(diphenylthiophosphoryl)ferrocene

被引：0
|
作者：
Michelot, Audric [1 ,2 ]
Sarda, Stephanie [3 ]
Daran, Jean-Claude [4 ]
Deydier, Eric [1 ,2 ]
Manoury, Eric [1 ,4 ]
机构：
[1] Univ Toulouse, UPS, INPT, F-31077 Toulouse 4, France
[2] CNRS, LCC, IUT, Dept Chim, F-81104 Castres, France
[3] Univ Toulouse 3, CIRIMAT, Equipe PPB, ENSIACET Bur 2r1 5, F-31432 Toulouse, France
[4] Lab Chim Coordinat, 205 Route Narbonne, F-31077 Toulouse 04, France
来源：
ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS | 2015年 / 71卷
关键词：
crystal structure; ferrocenyl ligands; planar chirality; asymmetric catalysis;
D O I：
10.1107/S2056989015013560
中图分类号：
O7 [晶体学];
学科分类号：
0702 ; 070205 ; 0703 ; 080501 ;
摘要：
The title compound, [Fe(C5H5)(C27H24OPS2)], is built up from a ferrocene moiety substituted in the 1- and 2-positions by {[4-(allyloxy)phenyl]sulfanyl} methyl and diphenylthiophosphoryl groups, respectively. The two S atoms lie on opposite sides of the cyclopentadienyl ring plane to which they are attached. In the crystal, C-H center dot center dot center dot S hydrogen bonds link the molecules into a ribbon running parallel to the ((1) over bar 10) plane. C-H center dot center dot center dot pi interactions link the ribbons to form a three-dimensional network.
引用
收藏
页码：972 / +
页数：11
相关论文
共 50 条
  • [41] 1-Methoxy-4-({[(4-methoxyphenyl)sulfanyl](phenyl) methyl} sulfanyl) benzene
    Li, Hongqi
    Ramachandran, G.
    Sathishkumar, M.
    Sathiyanarayanan, K.
    Rathore, R. S.
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O782 - U2582
  • [42] (±)-2-{[4-(4-Bromophenyl)-5-phenyl-4H-1,2,4-triazol-3-yl]sulfanyl}-1-phenyl-1-ethanol
    Vorga, Milenca Mariana
    Badea, Valentin
    MOLBANK, 2021, 2021 (03)
  • [43] Crystal structure of 1-[(E)-2-[4-(trifluoromethyl)phenyl]-1-ethenyl]-naphthalene, C19H13F3
    Jevric, M
    Taylor, DK
    Tiekink, ERT
    ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES, 2001, 216 (04): : 545 - 546
  • [44] Synthesis and Crystal Structure of 1-(4-{[(E)-4-methoxy-2-hydroxybenzylidene]amino}phenyl)ethanoe Oxime
    Dong, Wen-Kui
    Wu, Jun-Jiang
    Wang, Li
    Zhang, Yang
    Li, Xiang
    Li, Li
    ASIAN JOURNAL OF CHEMISTRY, 2013, 25 (11) : 6156 - 6158
  • [45] Synthesis,Crystal Structure and Neuroprotection of Methyl 2-((4-(2-(2-Methylphenoxy)acetyl)-piperazin-1-yl)-methyl)benzoate
    仲琰
    王垚
    王晶
    许逸
    李萍
    吴斌
    Chinese Journal of Structural Chemistry, 2014, 33 (07) : 1096 - 1101
  • [46] Design, synthesis, and evaluation of 4-[2-(diphenylmethoxy)ethyl]-1-[(phenyl)methyl]piperidine analogs for the dopamine transporter.
    Dutta, A
    Fei, XS
    Beardsley, P
    Reith, M
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 220 : U576 - U577
  • [47] 2-((E)-{[4-(Hydroxymethyl)phenyl]-imino}methyl)phenol
    Mohamed, Shaaban K.
    Abdelhamid, Antar A.
    Akkurt, Mehmet
    Fanwick, Phillip E.
    Maharramov, A. M.
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O1618 - +
  • [48] Diethyl 2-{(dibenzylamino)[4-(trifluoromethyl)phenyl]methyl}malonate
    Meskini, Ihssan
    Daoudi, Maria
    Daran, Jean-Claude
    Zouihri, Hafid
    Kerbal, Abdelali
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2010, 66 : O961 - U3412
  • [49] Synthesis of (2E)-2-methyl-3-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)prop-2-enoic acid (VUFB 20609) and 2-methyl-3-(4-{[4-(quinolin-2-ylmethoxy)phenyl]sulfanyl}phenyl)propanoic acid (VUFB 20584) as potential antileukotrienic agents
    Jampílek, J
    Dolezal, M
    Kunes, J
    Vichová, P
    Jun, D
    Hanika, J
    O'Connor, R
    Clynes, M
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2004, 56 (06) : 783 - 794
  • [50] Synthesis, characterization and in vitro antimicrobial activity of some 1-(substitutedbenzylidene)-4-(4-(2-(methyl/phenyl)-4-oxoquinazolin-3(4H)-yl)phenyl)semicarbazide derivatives
    Saravanan, Govindaraj
    Alagarsamy, Veerachamy
    Prakash, Chinnasamy Rajaram
    JOURNAL OF SAUDI CHEMICAL SOCIETY, 2015, 19 (01) : 3 - 11
12345