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Collect. Czech. Chem. Commun. 2000, 65, 1273-1288
https://doi.org/10.1135/cccc20001273

Molecular and Crystal Structure of Benzohydroxamic Acid and Its Ring-Substituted Derivatives

Jaroslav Podlahaa, Ivana Císařováa,*, Ludmila Soukupováb and Jan Schramlb

a Department of Inorganic Chemistry, Charles University, 128 40 Prague 2, Czech Republic
b Institute of Chemical Process Fundamentals, Academy of Sciences of the Czech Republic, 165 02 Prague 6, Czech Republic

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  • Rahman Md Lutfor, Sarjadi Mohd Sani, Sarkar Shaheen M., Walsh Daniel J., Hannan John J.: Poly(hydroxamic acid) resins and their applications. Coordination Chemistry Reviews 2022, 471, 214727. <https://doi.org/10.1016/j.ccr.2022.214727>
  • Watson Paris R., Bai Ping, Wang Changning, Cragin Abigail D., Hooker Jacob M., Christianson David W.: Aromatic Ring Fluorination Patterns Modulate Inhibitory Potency of Fluorophenylhydroxamates Complexed with Histone Deacetylase 6. Biochemistry 2022, 61, 1945. <https://doi.org/10.1021/acs.biochem.2c00332>
  • Rahman Md Lutfor, Sarjadi Mohd Sani, Sarkar Shaheen M., Walsh Daniel J., Hannan John J.: Poly(Hydroxamic Acid) Resins and Their Applications. SSRN Journal 2022. <https://doi.org/10.2139/ssrn.4059760>
  • He Jianyong, Zhou Qiqi, Chen Shengda, Tian Mengjie, Zhang Chenyang, Sun Wei: Interfacial microstructures and adsorption mechanisms of benzohydroxamic acid on Pb2+-activated cassiterite (1 1 0) surface. Applied Surface Science 2021, 541, 148506. <https://doi.org/10.1016/j.apsusc.2020.148506>
  • Saldyka Magdalena, Coussan Stéphane: Infrared spectra and photodecomposition of benzohydroxamic acid isolated in argon matrices. Journal of Molecular Structure 2020, 1219, 128506. <https://doi.org/10.1016/j.molstruc.2020.128506>
  • Codd Rachel: Traversing the coordination chemistry and chemical biology of hydroxamic acids. Coord Chem Rev - 2008, 252, 1387. <https://doi.org/10.1016/j.ccr.2007.08.001>
  • Yamasaki Ryu, Tanatani Aya, Azumaya Isao, Masu Hyuma, Yamaguchi Kentaro, Kagechika Hiroyuki: Solvent-Dependent Conformational Switching of N-Phenylhydroxamic Acid and Its Application in Crystal Engineering. Growth Des 2006, 6, 2007. <https://doi.org/10.1021/cg060151z>
  • Schraml Jan, Tkadlecová Marcela, Pataridis Statis, Soukupová Ludmila, Blechta Vratislav, Roithová Jana, Exner Otto: Ring‐substituted benzohydroxamic acids: 1H, 13C and 15N NMR spectra and NHOH proton exchange. Magnetic Reson in Chemistry 2005, 43, 535. <https://doi.org/10.1002/mrc.1586>
  • Gálvez Natividad, Ruiz Beatriz, Cuesta Rafael, Colacio Enrique, Domínguez-Vera José M.: Release of Iron from Ferritin by Aceto- and Benzohydroxamic Acids. Inorg. Chem. 2005, 44, 2706. <https://doi.org/10.1021/ic048840s>
  • Blajiev Orlin, Hubin Annick, Tielens Frederik, Geerlings Paul: Raman and DFT study of the vibrational properties of some para‐substituted benzohydroxamic acids: towards an interpretation of SER spectra. J Raman Spectroscopy 2003, 34, 295. <https://doi.org/10.1002/jrs.995>
  • Luzyanin Konstantin V., Kukushkin Vadim Yu., Kuznetsov Maxim L., Garnovskii Dmitrii A., Haukka Matti, Pombeiro Armando J. L.: Novel Reactivity Mode of Hydroxamic Acids:  A Metalla-Pinner Reaction. Inorg. Chem. 2002, 41, 2981. <https://doi.org/10.1021/ic025554c>
  • Remko Milan: The Gas-Phase Acidities of Substituted Hydroxamic and Silahydroxamic Acids:  A Comparative ab Initio Study. J. Phys. Chem. A 2002, 106, 5005. <https://doi.org/10.1021/jp020300y>
  • Schraml Jan, Soukupová Ludmila, Blechta Vratislav, Karban Jindřich, Cı́sařová Ivana: Structure of monosilylated benzhydroxamic acids in crystals and solutions. Journal of Organometallic Chemistry 2001, 628, 81. <https://doi.org/10.1016/S0022-328X(01)00762-8>
  • Hnyk Drahomír, Borisenko Konstantin B., Samdal Svein, Exner Otto: Structure of Methyl 2-Methylbenzoate: Steric Effect of a Smallortho-Substituent. Eur. J. Org. Chem. 2000, 2000, 2063. <https://doi.org/10.1002/1099-0690(200006)2000:11<2063::AID-EJOC2063>3.0.CO;2-0>