z-logo
Premium
System with Potential Dual Modes of Metal–Ligand Cooperation: Highly Catalytically Active Pyridine‐Based PNNH–Ru Pincer Complexes
Author(s) -
Fogler Eran,
Garg Jai Anand,
Hu Peng,
Leitus Gregory,
Shimon Linda J. W.,
Milstein David
Publication year - 2014
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201405295
Subject(s) - pincer movement , deprotonation , pincer ligand , chemistry , ligand (biochemistry) , ruthenium , catalysis , amide , pyridine , amine gas treating , aromatization , combinatorial chemistry , photochemistry , medicinal chemistry , organic chemistry , ion , biochemistry , receptor
Metal–ligand cooperation (MLC) plays an important role in catalysis. Systems reported so far are generally based on a single mode of MLC. We report here a system with potential for MLC by both amine–amide and aromatization–dearomatization ligand transformations, based on a new class of phosphino–pyridyl ruthenium pincer complexes, bearing sec ‐amine coordination. These pincer complexes are effective catalysts under unprecedented mild conditions for acceptorless dehydrogenative coupling of alcohols to esters at 35 °C and hydrogenation of esters at room temperature and 5 atm H 2 . The likely actual catalyst, a novel, crystallographically characterized monoanionic de‐aromatized enamido–Ru II complex, was obtained by deprotonation of both the NH and the methylene proton of the N‐arm of the pincer ligand.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom