LEADER 05364nam 2200673Ia 450 001 9910456159103321 005 20200520144314.0 010 $a1-282-75993-0 010 $a9786612759932 010 $a1-84816-412-2 035 $a(CKB)2490000000001631 035 $a(EBL)1681373 035 $a(SSID)ssj0000410521 035 $a(PQKBManifestationID)11268506 035 $a(PQKBTitleCode)TC0000410521 035 $a(PQKBWorkID)10353481 035 $a(PQKB)11325097 035 $a(MiAaPQ)EBC1681373 035 $a(WSP)00002055 035 $a(Au-PeEL)EBL1681373 035 $a(CaPaEBR)ebr10422389 035 $a(CaONFJC)MIL275993 035 $a(OCoLC)879025262 035 $a(EXLCZ)992490000000001631 100 $a20090825d2010 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$a1,1'-binaphthyl-based chiral materials$b[electronic resource] $eour journey /$fLin Pu 210 $aLondon $cImperial College Press$dc2010 215 $a1 online resource (346 p.) 300 $aDescription based upon print version of record. 311 $a1-84816-411-4 320 $aIncludes bibliographical references and index. 327 $aPreface; Contents; References; 1. Introduction About 1,1 -Binaphthyls; References; 2. Main Chain Chiral-Conjugated Polymers; 2.1. Introduction About Chiral-Conjugated Polymers; 2.2. Binaphthyl-Based Polyarylenevinylenes; 2.3. Binaphthyl-Based Polyarylenes; 2.4. Binaphthyl-Based Polyaryleneethynylenes; 2.5. Binaphthyl-Thiophene Copolymers; 2.5.1. Copolymerization of Binaphthyl and Oligothiophene Monomers; 2.5.2. Electroluminescence Study; 2.6. Copolymers of BINAM and Thiophene-Containing Conjugated Linkers; 2.7. Polybinaphthyls Without Conjugated Linkers 327 $a2.7.1. Using Nickel Complexes to Promote Polymerization212.7.2. Synthesis of the Binaphthyl-Based Polydendrimers by Using Ni Complexes to Promote Polymerization23; 2.7.3. Using the Suzuki Coupling Reaction for Polymerization21b; 2.7.4. Electroluminescence Study of the Polybinaphthyls26; 2.8. Propeller-Like Polybinaphthyls; 2.8.1. Synthesis of the Propeller-Like Polymers Derived from BINOL27,28; 2.8.2. Synthesis of the Propeller-Like Polymers Derived from BINAM31; 2.8.3. Study of the Non-linear Optical Properties of the Propeller-Like Polymers32; 2.9. Dipole-Oriented Propeller-Like Polymers 327 $a2.10. Binaphthyl-Based Polysalophens2.11. Helical Ladder Polybinaphthyls; References; 3. Polybinaphthyls in Asymmetric Catalysis; 3.1. Introduction about Chiral Polymers in Asymmetric Catalysis; 3.2. Synthesis of Major-Groove Poly(BINOL)s; 3.2.1. Synthesis of Polybinaphthyls with Various Protecting Groups5; 3.2.2. Hydrolysis of the Polybinaphthyls to Generate Poly(BINOL)s5; 3.2.3. Synthesis of Poly(BINOL)s Containing Alkyl-Substituted Phenylene Linkers6; 3.3. Application of the Major-Groove Poly(BINOL)s to Catalyze the Mukaiyama Aldol Reaction 327 $a3.4. Application of the Major-Groove Poly(BINOL)s to Catalyze the Hetero-Diels-Alder Reaction3.5. Using the Ti(IV) Complex of the Major-Groove Poly(BINOL) to Catalyze the Diethylzinc Addition to Aldehydes; 3.6. Synthesis of the Minor-Groove Poly(BINOL)s; 3.7. Application of the Major- and Minor-Groove Poly(BINOL)s to Catalyze the Asymmetric Organozinc Addition to Aldehydes; 3.7.1. Asymmetric Diethylzinc Addition to Aldehydes Catalyzed by the Poly(BINOL)s; 3.7.2. Study of the Reactions of the Minor-Groove Poly(BINOL) and a Few Monomeric BINOL Derivatives with Diethylzinc 327 $a3.7.3. Synthesis of the Monomeric Model Compound of the Minor-Groove Poly(BINOL) to Catalyze the Dialkylzinc Addition to Aldehydes10b,c3.7.4. Converting the Highly Enantioselective Mono(BINOL) Catalyst to a Highly Enantioselective Poly(BINOL) Catalyst for the Asymmetric Organozinc Additions10; 3.8. Asymmetric Reduction of Prochiral Ketones Catalyzed by the Chiral BINOL Monomer and Polymer Catalysts; 3.9. Asymmetric Epoxidation of ?, ?-UnsaturatedKetones Catalyzed by the Minor- and Major-GroovePoly(BINOL)s 327 $a3.9.1. Asymmetric Epoxidation of ?,?-Unsaturated Ketonesin the Presence of a Stoichiometric Amount of theMajor-Groove Poly(BINOL)s, Diethylzincand Oxygen 330 $aChiral 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. 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 processes. In this book, both the fundamental knowledge about the 1,1'-binaphthyl molecules and the sy 606 $aChirality 606 $aAsymmetric synthesis 606 $aMolecular theory 608 $aElectronic books. 615 0$aChirality. 615 0$aAsymmetric synthesis. 615 0$aMolecular theory. 676 $a547 700 $aPu$b Lin$f1965-$0992811 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910456159103321 996 $a1,1'-binaphthyl-based chiral materials$92273360 997 $aUNINA