Volume 25, Issue 5 pp. 390-394
Full Paper

Synthesis of new boron complexes: application to transfer hydrogenation of acetophenone derivatives

Ahmet Kilic

Corresponding Author

Ahmet Kilic

Harran University, Department of Chemistry, 63190, Sanliurfa, Turkey

Harran University, Department of Chemistry, 63190, Sanliurfa, Turkey.Search for more papers by this author
Cezmi Kayan

Cezmi Kayan

Dicle University, Department of Chemistry, 21280 Diyarbakır, Turkey

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Murat Aydemir

Murat Aydemir

Dicle University, Department of Chemistry, 21280 Diyarbakır, Turkey

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Feyyaz Durap

Feyyaz Durap

Dicle University, Department of Chemistry, 21280 Diyarbakır, Turkey

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Mustaf1 Durgun

Mustaf1 Durgun

Harran University, Department of Chemistry, 63190, Sanliurfa, Turkey

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Akın Baysal

Akın Baysal

Dicle University, Department of Chemistry, 21280 Diyarbakır, Turkey

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Esref Tas

Esref Tas

Siirt University, Department of Chemistry, 56100 Siirt, Turkey

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Bahattin Gümgüm

Bahattin Gümgüm

Dicle University, Department of Chemistry, 21280 Diyarbakır, Turkey

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First published: 04 April 2011
Citations: 31

Abstract

Two new boron complexes were synthesized from N-[3-(methylmercapto)aniline]-3,5-di-tert-butylsalicylaldimine (LH) with boron reagent BPh3 or BF3.Et2O. These boron complexes are stable and easily soluble in protic solvents such as ethanol (C2H5OH) but hardly soluble in nonprotic solvents such as chloroform (CHCl3), dichloromethane (CH2Cl2) and tetrahydrofuran (THF). All new boron complexes have been fully characterized by both analytical and spectroscopic methods. The catalytic activities of complexes [LBPh2], 2, and [LBF2], 3, in the transfer hydrogenation of acetophenone derivatives were tested. Stable boron complexes were found to be efficient catalysts in the transfer hydrogenation of aromatic ketones in good conversions up to 99% in the presence of iso-PrOH/KOH. Copyright © 2011 John Wiley & Sons, Ltd.

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