Triarylborane-functionalized polynorbornenes: Direct polymerization and signal amplification in fluoride sensing
暂无分享,去创建一个
M. H. Lee | Y. Do | Myung-Hwan Park | Jun Ha Park | Mee-Seon Yu | Maengsun Eo | W. Y. Sung
[1] O. Wenger,et al. Multistage complexation of fluoride ions by a fluorescent triphenylamine bearing three dimesitylboryl groups: controlling intramolecular charge transfer. , 2011, The Journal of organic chemistry.
[2] R. Lalancette,et al. Turn-on fluorescence response upon anion binding to dimesitylboryl-functionalized quaterthiophene. , 2011, Chemical communications.
[3] M. H. Lee,et al. Luminescent polyethylene with side-chain triarylboranes: Synthesis and fluoride sensing properties , 2011 .
[4] Changhun Yun,et al. Vinyl-type polynorbornene with 9,9′-(1,1′-biphenyl)-4,4′-diylbis-9H-carbazole side groups as a host material for highly efficient green phosphorescent organic light-emitting diodes , 2011 .
[5] M. H. Lee,et al. Metallocene-catalyzed synthesis of polyethylenes with side-chain triarylamines: Effects of catalyst structure and triarylamine functionality , 2010 .
[6] T. James,et al. Boron based anion receptors as sensors. , 2010, Chemical Society reviews.
[7] S. Yoo,et al. Synthesis and hole-transporting properties of vinyl-type polynorbornenes with ethyl ester linked triarylamine side groups , 2010 .
[8] Qiang Shi,et al. Boron-containing monopyrrolo-annelated tetra thiafulvalene compounds: synthesis and absorption spectral/electrochemical responsiveness toward fluoride ion. , 2010, The Journal of organic chemistry.
[9] C. Wade,et al. Fluoride ion complexation and sensing using organoboron compounds. , 2010, Chemical reviews.
[10] F. Jäkle. Advances in the synthesis of organoborane polymers for optical, electronic, and sensory applications. , 2010, Chemical reviews.
[11] Yoon Sup Lee,et al. o-Carborane-assisted Lewis acidity enhancement of triarylboranes. , 2010, Chemical communications.
[12] F. Jäkle,et al. Weakly coordinating amphiphilic organoborate block copolymers. , 2010, Journal of the American Chemical Society.
[13] C. Wade,et al. Cyanide anion binding by a triarylborane at the outer rim of a cyclometalated ruthenium(II) cationic complex. , 2010, Inorganic chemistry.
[14] S. Yoo,et al. Vinyl-Type Polynorbornenes with Triarylamine Side Groups: A New Class of Soluble Hole-Transporting Materials for OLEDs , 2009 .
[15] J. Kobayashi,et al. Enhancement of the Lewis acidity by substitution of sulfur-containing hetero aromatics in triarylboranes , 2009 .
[16] Suning Wang,et al. Impact of donor-acceptor geometry and metal chelation on photophysical properties and applications of triarylboranes. , 2009, Accounts of chemical research.
[17] K. Rissanen,et al. Recognition and sensing of fluoride anion. , 2009, Chemical communications.
[18] F. Jäkle,et al. Synthesis, Characterization, and Anion Binding of Redox-Active Triarylborane Polymers , 2009 .
[19] Y. Chujo,et al. Synthesis of Organoboron Quinoline-8-thiolate and Quinoline-8-selenolate Complexes and Their Incorporation into the π-Conjugated Polymer Main-Chain , 2009 .
[20] F. Jäkle,et al. Universal scaffold for fluorescent conjugated organoborane polymers. , 2009, Angewandte Chemie.
[21] F. Gabbaï,et al. Cationic boranes for the complexation of fluoride ions in water below the 4 ppm maximum contaminant level. , 2009, Journal of the American Chemical Society.
[22] F. Gabbaï,et al. Fluoride ion recognition by chelating and cationic boranes. , 2009, Accounts of chemical research.
[23] M. H. Lee,et al. Synthesis and properties of polyethylene with side‐chain triphenylamines as hole‐transporting materials , 2008 .
[24] A. Tani,et al. Synthesis of B/Si bidentate Lewis acids, o-(Fluorosilyl)(dimesitylboryl)benzenes, and their fluoride ion affinity. , 2008, Journal of the American Chemical Society.
[25] Y. Chujo,et al. Synthesis of New Main-Chain-Type Organoboron Quinolate Polymer Linked on Quinolate Ligand , 2008 .
[26] F. Gabbaï,et al. Ammonium boranes for the selective complexation of cyanide or fluoride ions in water. , 2007, Journal of the American Chemical Society.
[27] Y. Chung,et al. Polymerization of carboxylic ester functionalized norbornenes catalyzed by (η3‐allyl)palladium complexes bearing N‐heterocyclic carbene ligands , 2007 .
[28] A. Wakamiya,et al. Highly Emissive Poly(aryleneethynylene)s Containing 2,5-Diboryl-1,4-phenylene as a Building Unit , 2007 .
[29] K. Venkatasubbaiah,et al. Organoborane acceptor-substituted polythiophene via side-group borylation. , 2007, Journal of the American Chemical Society.
[30] Jianzhang Zhao,et al. Simple bis-thiocarbono-hydrazones as sensitive, selective, colorimetric, and switch-on fluorescent chemosensors for fluoride anions. , 2007, Chemistry.
[31] M. H. Lee,et al. Fluoride ion complexation by a cationic borane in aqueous solution. , 2007, Chemical communications.
[32] Y. Chujo,et al. Main-Chain-Type Organoboron Quinolate Polymers: Synthesis and Photoluminescence Properties , 2007 .
[33] Yang Qin,et al. Synthesis and Characterization of Organoboron Quinolate Polymers with Tunable Luminescence Properties , 2006 .
[34] K. Venkatasubbaiah,et al. Luminescent triarylborane-functionalized polystyrene: synthesis, photophysical characterization, and anion-binding studies. , 2006, Journal of the American Chemical Society.
[35] Suning Wang,et al. Charge-transfer emission in nonplanar three-coordinate organoboron compounds for fluorescent sensing of fluoride. , 2006, Angewandte Chemie.
[36] Eric Verploegen,et al. Synthesis and Characterization of ABA Triblock Copolymers Containing Smectic C* Liquid Crystal Side Chains via Ring-Opening Metathesis Polymerization Using a Bimetallic Molybdenum Initiator , 2006 .
[37] F. Jäkle. Lewis acidic organoboron polymers , 2006 .
[38] Christopher D. Entwistle,et al. Synthesis, crystal structures, linear and nonlinear optical properties, and theoretical studies of (p-R-phenyl)-, (p-R-phenylethynyl)-, and (E)-[2-(p-R-phenyl)ethenyl]dimesitylboranes and related compounds. , 2006, Chemistry.
[39] Yang Qin,et al. A synthetic route to borylene-bridged poly(ferrocenylene)s. , 2006, Angewandte Chemie.
[40] Yang Qin,et al. Preparation of organoboron block copolymers via ATRP of silicon and boron-functionalized monomers , 2005 .
[41] Y. Chujo,et al. Studies on electrical transport properties of a novel n-type polymer containing tripylborane and fluorene moieties , 2005 .
[42] F. Jäkle,et al. A family of main-chain polymeric Lewis acids: synthesis and fluorescent sensing properties of boron-modified polythiophenes. , 2005, Journal of the American Chemical Society.
[43] F. Jäkle. Borylated Polyolefins and their Applications , 2005 .
[44] M. Weck,et al. Poly(styrene)-Supported Alq3 and BPh2q , 2005 .
[45] N. Krause,et al. Studies on the synthesis of macrocyclic allenes by ring closing metathesis and Doering-Moore-Skattebøl reaction , 2005 .
[46] Yang Qin,et al. A New Route to Organoboron Polymers via Highly Selective Polymer Modification Reactions , 2004 .
[47] F. Gabbaï,et al. A bidentate borane as colorimetric fluoride ion sensor. , 2004, Chemical communications.
[48] C. Pagba,et al. Luminescent organoboron quinolate polymers. , 2004, Journal of the American Chemical Society.
[49] L. Cavallo,et al. Synthetic and Structural Studies of (NHC)Pd(allyl)Cl Complexes (NHC = N-heterocyclic carbene) , 2004 .
[50] S. Oh,et al. Structural effects of a light emitting copolymer having perylene moieties in the side chain on the electroluminescent characteristics , 2004 .
[51] J. Gabrilove,et al. Fluoride: A toxic or therapeutic agent in the treatment of osteoporosis? , 2004 .
[52] Y. Shirota,et al. Development of a new class of hole-transporting and emitting vinyl polymers and their application in organic electroluminescent devices , 2003 .
[53] Y. Chujo,et al. Synthesis of New Fluorescent Organoboron Polymers Based on Pyrazaboles , 2003 .
[54] Y. Ichikawa,et al. Electrical conductivity of π-conjugated organoboron polymers upon n-type doping , 2003 .
[55] M. Weck,et al. Towards a universal polymer backbone: design and synthesis of polymeric scaffolds containing terminal hydrogen-bonding recognition motifs at each repeating unit. , 2003, Chemistry.
[56] Y. Chujo,et al. π-Conjugated Organoboron Polymer as an Anion Sensor , 2002 .
[57] Yang Qin,et al. Well-defined boron-containing polymeric lewis acids. , 2002, Journal of the American Chemical Society.
[58] K. Tamao,et al. Colorimetric fluoride ion sensing by boron-containing pi-electron systems. , 2001, Journal of the American Chemical Society.
[59] Y. Chujo,et al. Facilitated dπ−pπ* Transition in a Novel Organoboron π-Conjugated Polymer Including a Ruthenium−Phosphine Complex , 2001 .
[60] N. Matsumi,et al. Synthesis of novel π-conjugated boron polymers containing transition metal in the main chain and their optical properties , 2001 .
[61] T. Umeyama,et al. Synthesis and Properties of Alternating Acceptor−Donor π-Conjugated Copolymers of Cyclodiborazane with Dithiafulvene , 2000 .
[62] N. Matsumi,et al. Novel π-conjugated organoboron polymers: Poly (ethynylene-phenylene-ethynylene-borane)s , 2000 .
[63] N. Matsumi,et al. π-Conjugated Poly(cyclodiborazane)s with Intramolecular Charge Transferred Structure , 2000 .
[64] Robert A. Shick,et al. Functionalized polynorbornene dielectric polymers: Adhesion and mechanical properties , 1999 .
[65] M. Large,et al. POLYURETHANES CONTAINING BORON CHROMOPHORES AS SIDECHAINS FOR NONLINEAR OPTICS , 1997 .
[66] J. Wendorff,et al. Polynorbornene: synthesis, properties and simulations , 1996 .
[67] Robert D. Miller,et al. Coupling reactions of higher order cuprates with primary halides: extremely mild and efficient substitution reactions of bromides and chlorides , 1983 .
[68] J. Lakowicz. Principles of fluorescence spectroscopy , 1983 .
[69] V. Gutmann,et al. The acceptor number — A quantitative empirical parameter for the electrophilic properties of solvents , 1975 .