Crystal structure and Hirshfeld surface analysis of 3-(3-hydroxyphenyl)-1-(1H-pyrrol-2-yl)prop-2-en1-one hemihydrate

被引:0
作者
Ismail, Ahmad Zaidi [1 ,2 ]
Gunasekharan, Mohanapriya [2 ]
Karunakaran, Thiruventhan [3 ]
Faudzi, Siti Munirah Mohd [2 ,4 ]
机构
[1] Univ Auckland, Sch Chem Sci, Private Bag 92019, Auckland, New Zealand
[2] Univ Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor, Malaysia
[3] Univ Sains Malaysia, Ctr Drug Res, Usm 11800, Pulau Pinang, Malaysia
[4] Univ Putra Malaysia, Inst Biosci, Nat Med & Prod Res Lab, Serdang 43400, Selangor, Malaysia
来源
ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS | 2023年 / 79卷
关键词
chalcone; pyrrole-derived chalcone; pyrrole; crystal structure; SCXRD; CHALCONE;
D O I
10.1107/S2056989023001925
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
High-quality single crystals of the title compound, 2C(13)H(11)NO(2).H2O, were grown and a structural analysis was performed. The asymmetric unit comprises one molecule of 3-(3-hydroxyphenyl)-1-(1H-pyrrol-2-yl)prop-2-en-1-one (3HPPP), which was recently discovered to be a promising anti-MRSA candidate, and a half-molecule of water. The compound crystallizes in the monoclinic space group P2/c. The crystal structure features intermolecular pyrrole-N-H...O (water), carbonyl/keto-C-O...H-O-phenol and phenolC-O...H (water) hydrogen bonds, which help to consolidate the crystal packing. A Hirshfeld surface analysis for the components in the asymmetric unit showed that H...H (40.9%) and H. ..C/C...H (32.4%) contacts make the largest contributions to the intermolecular interactions of 3HPPP. Considering the presence of water, in its vicinity H...O/O...H and H...C/C...H are the most significant contacts, contributing 48.7 and 29.8%, respectively.
引用
收藏
页码:287 / +
页数:9
相关论文
共 21 条
  • [11] Chalcones and flavonoids as anti-tuberculosis agents
    Lin, YM
    Zhou, YS
    Flavin, MT
    Zhou, LM
    Nie, WG
    Chen, FC
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2002, 10 (08) : 2795 - 2802
  • [12] An updated patent review of therapeutic applications of chalcone derivatives (2014-present)
    Mahapatra, Debarshi Kar
    Asati, Vivek
    Bharti, Sanjay Kumar
    [J]. EXPERT OPINION ON THERAPEUTIC PATENTS, 2019, 29 (05) : 385 - 406
  • [13] The self-assembly and spontaneous resolution of a hydrogen-bonded helix
    Norsten, TB
    McDonald, R
    Brenda, NR
    [J]. CHEMICAL COMMUNICATIONS, 1999, (08) : 719 - 720
  • [14] A review of anti-infective and anti-inflammatory chalcones
    Nowakowska, Zdzislawa
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2007, 42 (02) : 125 - 137
  • [15] Rigaku OD, 2021, CRYSALIS PRO
  • [16] SHELXT - Integrated space-group and crystal-structure determination
    Sheldrick, George M.
    [J]. ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2015, 71 : 3 - 8
  • [17] Sheldrick GM, 2015, ACTA CRYSTALLOGR C, V71, P3, DOI [10.1107/S2053273314026370, 10.1107/S2053229614024218, 10.1107/S0108767307043930]
  • [18] CrystalExplorer: a program for Hirshfeld surface analysis, visualization and quantitative analysis o molecular crystals
    Spackman, Peter R.
    Turner, Michael J.
    McKinnon, Joshua J.
    Wolff, Stephen K.
    Grimwood, Daniel J.
    Jayatilaka, Dylan
    Spackman, Mark A.
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2021, 54 : 1006 - 1011
  • [19] Chalcone derivatives as fluorescence turn-on chemosensors for cyanide anions
    Sun, Yunhui
    Chen, Huihui
    Cao, Duxia
    Liu, Zhiqiang
    Chen, Hongyu
    Deng, Yunlong
    Fang, Qi
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2012, 244 : 65 - 70
  • [20] publCIF: software for editing, validating and formatting crystallographic information files
    Westrip, Simon P.
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2010, 43 : 920 - 925