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A Modular Approach to Structurally Diverse Bidentate Chelate Ligands for Transition Metal Catalysis
Author(s) -
Kranich Remo,
Eis Knut,
Geis Oliver,
Mühle Stefan,
Bats Jan W.,
Schmalz HansGünther
Publication year - 2000
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 - 10.1002/1521-3765(20000804)6:15<2874::aid-chem2874>3.0.co;2-1
Subject(s) - denticity , chelation , transition metal , modular design , catalysis , combinatorial chemistry , chemistry , metal , stereochemistry , computer science , organic chemistry , operating system
A modular approach to a new class of structurally diverse bidentate P/N, P/P, P/S, and P/Se chelate ligands has been developed. Starting from hydroquinone, various ligands were synthesized in a divergent manner via orthogonally bis‐protected bromohydroquinones as the central building block. The first donor functionality (L 1 ) is introduced to the aromatic (hydroquinone) ligand backbone either by Pd‐catalyzed cross‐coupling (Suzuki coupling) with hetero‐aryl bromides, by Pd‐catalyzed amination, or by lithiation and subsequent treatment with electrophiles (e.g., chlorophosphanes, disulfides, diselenides, or carbamoyl chlorides). After selective deprotection, the second ligand tooth (L 2 ) is attached by reaction of the phenolic OH functionality with a chlorophosphane, a chlorophosphite, or a related reagent. Some of the resulting chelate ligands were converted into the respective PdX 2 complexes (X=Cl, I), two of which were characterized by X‐ray crystallography. The methodology developed opens an access to a broad variety of new chiral and achiral transition metal complexes and is generally suited for the solid‐phase synthesis of combinatorial libraries, as will be reported separately.