Literature DB >> 12526406

A study of the sequential acid-catalyzed hydroxylation of dodecahydro-closo-dodecaborate(2-).

T Peymann1, C B Knobler, M F Hawthorne.   

Abstract

The closo-[B12H12-n(OH)n]2- (n = 1-4) ions have been synthesized by the reaction of cesium dodecahydro-closo-dodecaborate(2-), Cs21, with aqueous sulfuric acid. Variation of the reaction temperature, time, and acid concentration results in the stepwise introduction of from one to four hydroxyl groups. Each individual hydroxylation step proceeds regioselectively, affording only one isomer per step. Further substitution of the hydroxylated cluster preferentially takes place at a B-H vertex meta to a B-OH vertex. The closo-[B12H12-n(OH)n]2- (n = 1-4) species, designated 2-5, respectively, are characterized by one- and two-dimensional 11B NMR spectroscopy, IR spectroscopy, and high-resolution fast atom bombardment (FAB) mass spectrometry. A rationale that qualitatively explains the influence of the hydroxyl group on the chemical shifts of the individual boron vertices is developed. Furthermore, the solid state structures of closo-[B12H11(OH)]2-, 2, and closo-1,7-[B12H10(OH)2]2-,3, are determined by X-ray diffraction. Crystallographic data are as follows: For [MePPh3](2)2, monoclinic, space group P2(1)/n, a = 890.1(5) pm, b = 1814(1) pm, c = 1270.5(7) pm, beta = 101.66(2) degrees, Z = 2, R = 0.055; for [MePPh3](2)3, monoclinic, space group P2(1)/n, a = 887.6(4) pm, b = 1847.2(8) pm, c = 1271.1(5) pm, beta = 101.17(1) degrees, Z = 2, R = 0.065. In addition, synthetic routes to O-derivatized species of the anions 2-5 such as closo-[B12H11(OTiCpCl2)]2-, 7, closo-1,7-[B12H10(OTiCpCl2)2]2-, 8, closo-1,7,9-[B12H9(OTiCpCl2)3]2-, 9, closo-[B12H11(OCONHPh)]2-, 10, and closo-1,7-[B12H10(OSO2Me)2]2-, 11, are described. The crystal structures of 7 and 11 are determined by single-crystal X-ray diffraction. Crystallographic data are as follows: For [MePPh3](2)7, monoclinic, space group Cc, a = 2530.5(2) pm, b = 1653.3(1) pm, c = 1281.3(1) pm, beta = 118.79(2) degrees, Z = 4, R = 0.085; for [HPy](2)11, monoclinic, space group P2(1)/n, a = 1550.9(8) pm, b = 993.1(5) pm, c = 1726.5(9) pm, beta = 112.36(2) degrees, Z = 4, R = 0.061.

Entities:  

Year:  2000        PMID: 12526406     DOI: 10.1021/ic991105+

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  2 in total

1.  Extensions of the icosahedral closomer structure by using azide-alkyne click reactions.

Authors:  Lalit N Goswami; Shatadru Chakravarty; Mark W Lee; Satish S Jalisatgi; M Frederick Hawthorne
Journal:  Angew Chem Int Ed Engl       Date:  2011-04-08       Impact factor: 15.336

2.  Ex Vivo and In Vivo Evaluation of Dodecaborate-Based Clusters Encapsulated in Ferumoxytol Nanoparticles.

Authors:  Nicholas A Bernier; James Teh; Derek Reichel; Joanne L Zahorsky-Reeves; J Manuel Perez; Alexander M Spokoyny
Journal:  Langmuir       Date:  2021-11-29       Impact factor: 3.882

  2 in total

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