Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid)
Reactions of a mononuclear molybdenum(V) starting material, (PyH)5[MoOCl4(H2O)]3Cl2, with 2,2-dimethylsuccinic acid in the presence of base afforded two products, (PyH)3[Mo2O4Cl4(μ2-dmsH)]·1/2CH3CN (1) and (PyH)4[Mo2O4Cl4(μ2-dmsH)]Cl (2). As revealed by the X-ray structure analysis, the half-neutral...
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MDPI AG
2013-04-01
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author | Barbara Modec |
author_facet | Barbara Modec |
author_sort | Barbara Modec |
collection | DOAJ |
description | Reactions of a mononuclear molybdenum(V) starting material, (PyH)5[MoOCl4(H2O)]3Cl2, with 2,2-dimethylsuccinic acid in the presence of base afforded two products, (PyH)3[Mo2O4Cl4(μ2-dmsH)]·1/2CH3CN (1) and (PyH)4[Mo2O4Cl4(μ2-dmsH)]Cl (2). As revealed by the X-ray structure analysis, the half-neutralized form of the dicarboxylic acid, the dmsH− ion, coordinated to the well-known {Mo2O4}2+ core in the syn-syn bidentate bridging manner. In both compounds, the non-ionized terminus of the ligand, the COOH function, participated in hydrogen-bonding interactions. The incorporation of the chloride counteranion in 2, prevented the formation of the common “carboxylic acid dimer” which was observed for 1. Instead, a hydrogen-bonded linkage of the COOH function with the chloride occurred. |
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publisher | MDPI AG |
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spelling | doaj.art-ea27b55f09c54fffaa13832769c379682022-12-22T03:09:53ZengMDPI AGCrystals2073-43522013-04-013227528810.3390/cryst3020275Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid)Barbara ModecReactions of a mononuclear molybdenum(V) starting material, (PyH)5[MoOCl4(H2O)]3Cl2, with 2,2-dimethylsuccinic acid in the presence of base afforded two products, (PyH)3[Mo2O4Cl4(μ2-dmsH)]·1/2CH3CN (1) and (PyH)4[Mo2O4Cl4(μ2-dmsH)]Cl (2). As revealed by the X-ray structure analysis, the half-neutralized form of the dicarboxylic acid, the dmsH− ion, coordinated to the well-known {Mo2O4}2+ core in the syn-syn bidentate bridging manner. In both compounds, the non-ionized terminus of the ligand, the COOH function, participated in hydrogen-bonding interactions. The incorporation of the chloride counteranion in 2, prevented the formation of the common “carboxylic acid dimer” which was observed for 1. Instead, a hydrogen-bonded linkage of the COOH function with the chloride occurred.http://www.mdpi.com/2073-4352/3/2/275molybdenum{Mo2O4}2+ corecarboxylate complexeshydrogen-bondingcarboxylic acid dimer |
spellingShingle | Barbara Modec Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid) Crystals molybdenum {Mo2O4}2+ core carboxylate complexes hydrogen-bonding carboxylic acid dimer |
title | Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid) |
title_full | Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid) |
title_fullStr | Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid) |
title_full_unstemmed | Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid) |
title_short | Hydrogen-Bonding in Two Pyridinium Salts of [Mo2O4Cl4(μ2-dmsH)]3−Complex (dmsH− = a Half-Neutralized Form of 2,2-Dimethylsuccinic Acid) |
title_sort | hydrogen bonding in two pyridinium salts of mo2o4cl4 μ2 dmsh 3 complex dmsh a half neutralized form of 2 2 dimethylsuccinic acid |
topic | molybdenum {Mo2O4}2+ core carboxylate complexes hydrogen-bonding carboxylic acid dimer |
url | http://www.mdpi.com/2073-4352/3/2/275 |
work_keys_str_mv | AT barbaramodec hydrogenbondingintwopyridiniumsaltsofmo2o4cl4m2dmsh3complexdmshahalfneutralizedformof22dimethylsuccinicacid |