Synthesis, spectroscopic characterization and thermal behavior of metal complexes formed with (Z)-2-oxo-2-(2-(2-oxoindolin-3-ylidene)hydrazinyl)-N-phenylacetamide (H2OI)

被引:58
|
作者
Yousef, T. A.
Rakha, T. H. [1 ]
El Ayaan, Usama [1 ]
Abu El Reash, G. M. [1 ]
机构
[1] Mansoura Univ, Fac Sci, Dept Chem, Mansoura 35516, Egypt
关键词
Hydrazone derivatives; Metal complexes; Thermal analysis; PM3; SCHIFF-BASE COMPLEXES; COPPER(II) COMPLEXES; ELECTRONIC-STRUCTURE; MAGNETIC-PROPERTIES; NICKEL(II); COBALT(II); SPECTRA; CU(II); STEREOCHEMISTRY; HYDRAZONE;
D O I
10.1016/j.molstruc.2011.10.036
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Complexes of Co(II), Ni(II), Cu(II), Cd(II), Zn(II) and U(IV)O-2 with (Z)-2-oxo-2-(2-(2-oxoindolin-3-ylidene)hydrazinyl)-N-phenylacetamide (H2OI) are reported and have been characterized by various spectroscopic techniques like (IR, UV-Vis, ESR H-1 and C-13 NMR) as well as magnetic and thermal (TG and DTA) measurements. It is found that the ligand behaves as a neutral tridentate, neutral tetradentate, monoanionic tridentate, monoanionic tridentate and dianionic tridentate. An octahedral geometry for all complexes except [Cu-2(H2OI)(OAc)(4)](H2O)(2) and [Cu(HOI)Cl](H2O)(2) which have a square planar geometry. Furthermore, kinetic parameters were determined for each thermal degradation stage of some studied complexes using Coats-Redfern and Horowitz-Metzger methods. The bond lengths, bond angles, HOMO, LUMO and dipole moments have been calculated to confirm the geometry of the ligand and the investigated complexes. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 157
页数:12
相关论文
共 50 条
  • [31] Synthesis, Spectroscopic Identification and Molecular Docking of Certain N-(2-{[2-(1H-Indol-2-ylcarbonyl) hydrazinyl](oxo)acetyl}phenyl)acetamides and N-[2-(2-{[2-(Acetylamino)phenyl](oxo)acetyl}hydrazinyl)-2-oxoethyl]-1H-indole-2-carboxamides: New Antimicrobial Agents
    Almutairi, Maha S.
    Zakaria, Azza S.
    Al-Wabli, Reem I.
    Joe, I. Hubert
    Abdelhameed, Ali S.
    Attia, Mohamed I.
    MOLECULES, 2018, 23 (05):
  • [32] Synthesis, Characterization, on, and Bioactivity Assessment of Rh(III) and VO(IV) Complexes with Isatin Derivative N1 , N2-bis(2-oxoindolin-3-ylidene)ethanebis(thioamide)
    Ahmed, Yusra Jalil
    Hasan, Shurooq Abdulfattah
    Hamud, Waeel Mohammed
    Mahmoud, Nawal Hamdan
    INDONESIAN JOURNAL OF CHEMISTRY, 2024, 24 (04) : 1091 - 1102
  • [33] Synthesis, Characterization, and Anti-Cancer Activity of Some New N'-(2-Oxoindolin-3-ylidene)-2-propylpentane hydrazide-hydrazones Derivatives
    El-Faham, Ayman
    Farooq, Muhammad
    Khattab, Sherine N.
    Abutaha, Nael
    Wadaan, Mohammad A.
    Ghabbour, Hazem A.
    Fun, Hoong-Kun
    MOLECULES, 2015, 20 (08): : 14638 - 14655
  • [34] Solubility and solvation behavior of N′-(1-(N-(methyl) benzylaminomethyl)-2-oxoindolin-3-ylidene)-2-(benzyloxy) benzohydrazide in (PEG 400+water) mixtures
    Shakeel, Faiyaz
    Haq, Nazrul
    Radwan, Awwad A.
    Alanazi, Fars K.
    Alsarra, Ibrahim A.
    JOURNAL OF MOLECULAR LIQUIDS, 2016, 221 : 1225 - 1230
  • [35] Crystal structure of (Z)-2-(1-benzyl-2-oxoindolin-3-ylidene)-N-phenylhydrazine-1-carbothioamide
    Vimala, G.
    Haribabu, J.
    Karvembu, R.
    Kumar, B. V. N. Phani
    SubbiahPandi, A.
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2015, 71 : O160 - +
  • [36] Nano SiO2 Catalyzed Chemo-Selective Synthesis of N′-Benzylidene-2-cyano-2-(10-oxophenanthren-9(10H)-ylidene) or (2-Oxoindolin-3-ylidene)acetohydrazide Derivatives
    Hosseini, Hajar
    Bayat, Mohammad
    CHEMISTRYSELECT, 2021, 6 (45): : 12884 - 12889
  • [37] Development of certain novel N-(2-(2-(2-oxoindolin-3-ylidene)hydrazinecarbonyl)phenyl)-benzamides and 3-(2-oxoindolin-3-ylideneamino)-2-substituted quinazolin-4(3H)-ones as CFM-1 analogs: Design, synthesis, QSAR analysis and anticancer activity
    Alafeefy, Ahmed M.
    Ashour, Abdelkader E.
    Prasad, Onkar
    Sinha, Leena
    Pathak, Shilendra
    Alasmari, Fatimah A.
    Rishi, Arun K.
    Abdel-Aziz, Hatem A.
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2015, 92 : 191 - 201
  • [38] Crystal structure of (Z)-methyl N′-(5,7-dibromo-1-(2-morpholinoethyl)-2-oxoindolin-3-ylidene)hydrazinecarbodithioate, C16H18Br2N4O2S2
    Ma, Li
    Li, Ai-Min
    Wan, Chong-Qing
    Cao, Sheng-Li
    ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES, 2014, 229 (01): : 25 - 26
  • [39] Target β-catenin/CD44/Nanog axis in colon cancer cells by certain N′-(2-oxoindolin-3-ylidene)-2-(benzyloxy)benzohydrazides
    Radwan, Awwad A.
    Al-Mohanna, F.
    Alanazi, Fares K.
    Manogaran, P. S.
    Al-Dhfyan, Abdullah
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, 26 (07) : 1664 - 1670
  • [40] Design, synthesis, and biological evaluation of 2-(2-oxoindolin-3-ylidene) hydrazinecarbothioamides as a potential EGR-1 inhibitor for targeted therapy of atopic dermatitis
    Ahn, Seunghyun
    Yeo, Hyunjin
    Jung, Euitaek
    Lee, Youngshim
    Koh, Dongsoo
    Lee, Hyeonhwa
    Lee, Young Han
    Lim, Yoongho
    Shin, Soon Young
    BIOORGANIC CHEMISTRY, 2024, 148