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Cage complexes as a molecular scaffold for polyfunctional and polytopic systems: Synthesis of the first closo-borate iron(II) clathrochelate

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Abstract

The ribbed functionalization of the clathrochelate iron(II) tris-dioximates as a potential “molecular scaffold” for the synthesis of polyfunctional and polytopic complexes with closo-dodecaborate-anion substituents was performed. closo-Dodecaborate-substituted clathrochelate [FeBd2(Cl(B12H11NH)Gm)(BF)2]2− (where Bd2− is α-benzyldioxime dianion, Gm is glyoxime residue) dianion was prepared starting from dichloride clathrochelate FeBd2(Cl2Gm)(BF)2 precursor with amino-closo-dodecaborate (NBu4)[B12H11NH3] in the presence of potassium tert-amylate. This clathrochelate dianion was isolated as a tetra-n-butylammonium salt and characterized using elemental analysis, MALDI-TOF and PD mass, IR, UV-Vis, 57Fe Mössbauer spectra as well as by 1H, 11B and 13C{1H} NMR spectra.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 21–24, January, 2006.

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Voloshin, Y.Z., Varzatskii, O.A., Zhizhin, K.Y. et al. Cage complexes as a molecular scaffold for polyfunctional and polytopic systems: Synthesis of the first closo-borate iron(II) clathrochelate. Russ Chem Bull 55, 22–25 (2006). https://doi.org/10.1007/s11172-006-0210-6

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  • DOI: https://doi.org/10.1007/s11172-006-0210-6

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