Includes bibliographical references and index.
|LC Classifications||QD481 .P88 2010|
|The Physical Object|
|Pagination||ix, 335 p. :|
|Number of Pages||335|
|LC Control Number||2010287992|
This book will serve as a reference for graduate students as well as other professionals working in the related fields. , ,, Reviews (0) Reviews There are no reviews yet. Be the first to review “1,1′ . 1,1'-binaphthyl-based Chiral Materials: Our Journey quantity. Add to cart. The applications of these materials in various fields are also discussed. This book will serve as a reference for graduate students as well as other professionals working in the related fields. , ,, Describes the synthesis and characterization of diverse materials based on the chiral, 1, 1'-binaphthyl structure. This book discusses the applications of these materials in various fields. It is suitable for graduate students as well as professionals working in the related fields. Optically active 1,1′-binaphthyl molecules are used to build novel chiral polymers, dendrimers, macrocycles, and acyclic molecules. 1,1′-Binaphthyl molecules are chosen because of their remarkably stable chiral configuration as well as their high asymmetric inductions in many this book, both the fundamental knowledge about the.
Get this from a library! 1,1'-binaphthyl-based chiral materials: our journey. [Lin Pu; World Scientific (Firm)] -- Chiral materials have been studied in the Department of Chemistry at the University of Virginia for applications in areas like asymmetric catalysis, enantioselective fluorescent sensing, and. 1, 1-binaphthyl-based Chiral Materials: Our Journey Lin Pu Chiral materials have been studied in the Department of Chemistry at the University of Virginia for applications in areas like asymmetric catalysis, enantioselective fluorescent sensing, and optical/electrical materials. This allows the isolation of the optically active 1,1'-binaphthyl enantiomers. A chiral 1,1'-binaphthyl molecule contains a chiral axis instead of a chiral center. The racemization half-life of the optically active 1,1'-binaphthyl was min at 50°C. 1,1'-Binaphthyls have two . 1, 1'-Binaphthyl-Based Chiral Materials Author: Lin Pu ISBN: Format: Hardcover Number Of Pages: Published: 1 August Country of Publication: GB Dimensions (cm): x x Description.
New chiral conjugated polymers and dendrimers are prepared for applications in materials, catalysis, and sensing. Book. 1,1'-BINAPHTHYL-BASED CHIRAL MATERIALS: OUR . In our laboratory, we have used optically active 1,1′-binaphthyl molecules to build new chiral materials because of the stable chiral configuration of the binaphthyl compounds and their high asymmetric induction in many processes,. Fig. 1 shows a few examples of the 1,1′-binaphthyl-based polymers prepared in our laboratory. Polymer 1 can catalyze several highly Cited by: In this book, both the fundamental knowledge about the 1,1′-binaphthyl molecules and the synthesis of the structurally diverse 1,1′-binaphthyl-based materials are described. These chiral compounds are potentially multifunctional materials bearing NLO responses. On the basis of this structural regime, we design several analogs (compounds 4, 5, and 6 in Fig. 1) by introducing different electron acceptors and donors on 2,2′-sites of 1,1′-binaphthyl to investigate the influence of electron acceptor–donor Cited by: