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Facile Conversion of Alcohols into Esters and Dihydrogen Catalyzed by New Ruthenium Complexes

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TLDR
In this paper, an efficient, environmentally benign method for the preparation of esters from alcohols under mild, neutral conditions without the need for carboxylic acid derivatives and condensing agents was developed.
Abstract
An efficient, environmentally benign method for the preparation of esters from alcohols under mild, neutral conditions without the need for carboxylic acid derivatives and condensing agents was developed. Catalyst design, based on new Ru(II) hydrido carbonyl complexes incorporating electron-rich PNP and PNN ligands has resulted in the novel complex (I) which is an outstanding catalyst for the dehydrogenation of primary alcohols to esters and H2 under neutral conditions.

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Citations
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Journal ArticleDOI

Reversible Hydrogen Activation by a Pyridonate Borane Complex: Combining Frustrated Lewis Pair Reactivity with Boron-Ligand Cooperation.

TL;DR: DFT and DLPNO-CCSD(T) computations reveal that the active form of the pyridonate borane complex is a boroxypyridine that can be described as a single component frustrated Lewis pair (FLP), and this unprecedented mode of action may be regarded as an example of boron-ligand cooperation.
Journal ArticleDOI

Facile Conversion of Alcohols into Esters and Dihydrogen Catalyzed by New Ruthenium Complexes.

TL;DR: In this article, an efficient, environmentally benign method for the preparation of esters from alcohols under mild, neutral conditions without the need for carboxylic acid derivatives and condensing agents was developed.
Patent

Novel ruthenium complexes and their uses in processes for formation and/or hydrogenation of esters, amides and derivatives thereof

TL;DR: In this article, the use of pyridine Ruthenium catalysts and related borohydride complexes has been investigated for hydrogenation of amides to alcohols and amines.
Journal ArticleDOI

Chromium(II) Pincer Complexes with Dearomatized PNP and PNC Ligands: A Comparative Study of Their Catalytic Ethylene Oligomerization Activity

TL;DR: In this paper, the 2,6-bis(di-tert-butylphosphinomethyl) pyridine (tBuPNtBuP) was modelled at the α-lutidinyl-CH2 position with 1 equiv of KCH2C6H5 and concomitant dearomatization of the heterocycle.
References
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Journal ArticleDOI

Direct Condensation of Carboxylic Acids with Alcohols Catalyzed by Hafnium(IV) Salts

TL;DR: It is shown that the direct condensation of equimolar amounts of carboxylic acids and alcohols can be achieved with the use of hafnium(IV) salts, such as commercially available ha fnium( IV) chloride and hafnia(IV), which may be suitable for large-scale operations.
Journal ArticleDOI

Electron-Rich, Bulky Ruthenium PNP-Type Complexes. Acceptorless Catalytic Alcohol Dehydrogenation

TL;DR: In this article, the electron-rich, bulky tridentate PNP ligand (2,6-bis-(di-tert-butylphosphinomethyl)pyridine) with Ru(PPh3)3Cl2 at 65 °C resulted in formation of a solution containing the dinitrogen monomeric Ru(II) complex 1a and the N2-bridged dinuclear Ru(2) complex 2, which can be interconverted.
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