Literature DB >> 11241595

Hemilability of Hybrid Ligands and the Coordination Chemistry of Oxazoline-Based Systems.

Pierre Braunstein1, Frédéric Naud.   

Abstract

Ligand design is becoming an increasingly important part of the synthetic activity in chemistry. This is of course because of the subtle control that ligands exert on the metal center to which they are coordinated. Ligands which contain significantly different chemical functionalities, such as hard and soft donors, are often called hybrid ligands and find increasing use in molecular chemistry. Although the interplay between electronic and steric properties has long been recognized as essential in determining the chemical or physical properties of a complex, predictions remain very difficult, not only because of the considerable diversity encountered within the Periodic Table-different metal centers will behave differently towards the same ligand and different ligands can completely modify the chemistry of a given metal-but also because of the small energy differences involved. New systems may-even through serendipity-allow the emergence of useful concepts that can gain general acceptance and help design molecular structures orientated towards a given property. The concept of ligand hemilability, which finds numerous illustrations with hybrid ligands, has gained increased acceptance and been found to be very useful in explaining the properties of metal complexes and in designing new systems for molecular activation, homogeneous catalysis, functional materials, or small-molecule sensing. In the field of homogeneous enantioselective catalysis, in which steric and/or electronic control of a metal-mediated process must occur in such a way that one stereoisomer is preferentially formed, ligands containing one or more chiral oxazoline units have been found to be very valuable for a wide range of metal-catalyzed reactions. The incorporation of oxazoline moieties in multifunctional ligands of increasing complexity makes such ligands good candidates to display hemilabile properties, which until recently, had not been documented in oxazoline chemistry. Herein, we briefly recall the definition and scope of hemilabile ligands, present the main classes of ligands containing one or more oxazoline moieties, with an emphasis on hybrid ligands, and finally explain why the combination of these two facets of ligand design appears particularly promising.

Entities:  

Year:  2001        PMID: 11241595     DOI: 10.1002/1521-3773(20010216)40:4<680::aid-anie6800>3.0.co;2-0

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  29 in total

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Authors:  Juan José Nuricumbo-Escobar; Carlos Campos-Alvarado; Gustavo Ríos-Moreno; David Morales-Morales; Patrick J Walsh; Miguel Parra-Hake
Journal:  Inorg Chem       Date:  2007-06-20       Impact factor: 5.165

2.  Hemilabile Proton Relays and Redox Activity Lead to {FeNO} x and Significant Rate Enhancements in NO2- Reduction.

Authors:  Pui Man Cheung; Kyle T Burns; Yubin M Kwon; Megan Y Deshaye; Kristopher J Aguayo; Victoria F Oswald; Takele Seda; Lev N Zakharov; Tim Kowalczyk; John D Gilbertson
Journal:  J Am Chem Soc       Date:  2018-11-30       Impact factor: 15.419

3.  Sodium Diisopropylamide: Aggregation, Solvation, and Stability.

Authors:  Russell F Algera; Yun Ma; David B Collum
Journal:  J Am Chem Soc       Date:  2017-05-30       Impact factor: 15.419

4.  Cyclic C-amino phosphorus ylides as a source of bidentate heteroditopic ligands (phosphine/aminocarbene) for transition metals.

Authors:  Joan Vignolle; Bruno Donnadieu; Didier Bourissou; Michèle Soleilhavoup; Guy Bertrand
Journal:  J Am Chem Soc       Date:  2006-11-22       Impact factor: 15.419

5.  Concise methods for the synthesis of chiral polyoxazolines and their application in asymmetric hydrosilylation.

Authors:  Wei Jie Li; Zun Le Xu; Sheng Xiang Qiu
Journal:  Beilstein J Org Chem       Date:  2010-03-25       Impact factor: 2.883

6.  cis-Bis-[2-(diphenyl-phosphino)benzene-thiolato-κP,S]palladium(II).

Authors:  Jaime Fierro-Arias; David Morales-Morales; Simón Hernández-Ortega
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-08-23

7.  rac-Carbon-yl{1-[(diphenyl-phosphino)meth-yl]ethanethiol-ato}(triphenyl-phosphine)rhodium(I).

Authors:  Simón Hernández-Ortega; David Morales-Morales
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-10-25

8.  Anionic Snieckus-Fries rearrangement: solvent effects and role of mixed aggregates.

Authors:  Jason C Riggs; Kanwal J Singh; Ma Yun; David B Collum
Journal:  J Am Chem Soc       Date:  2008-09-18       Impact factor: 15.419

9.  Lithium enolates of simple ketones: structure determination using the method of continuous variation.

Authors:  Lara R Liou; Anne J McNeil; Antonio Ramirez; Gilman E S Toombes; Jocelyn M Gruver; David B Collum
Journal:  J Am Chem Soc       Date:  2008-03-13       Impact factor: 15.419

10.  Harnessing the active site triad: merging hemilability, proton responsivity, and ligand-based redox-activity.

Authors:  Douglas F Baumgardner; Wyatt E Parks; John D Gilbertson
Journal:  Dalton Trans       Date:  2020-01-07       Impact factor: 4.390

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