Literature DB >> 12203415

Boron chemistry lights the way: optical properties of molecular and polymeric systems.

Christopher D Entwistle1, Todd B Marder.   

Abstract

Electrooptical and electronic materials are the subject of much research interest, whereby the focus has often been on electron-rich organic molecules. In the past years, new routes to electron-deficient systems have been developed that take advantage of the fact that three-coordinate boron is isoelectronic and isostructural with a positively charged carbocation, which allows neutral, p-type materials to be synthesized directly. This minireview summarizes recent work on compounds with 3- and 4-coordinate boron as well as boron clusters, placing it in the context of prior studies by the research groups of Williams and Glowgowski, Kaim, Lequan, and Marder.

Entities:  

Year:  2002        PMID: 12203415     DOI: 10.1002/1521-3773(20020816)41:16<2927::AID-ANIE2927>3.0.CO;2-L

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


  37 in total

1.  Nonlinear Optical Properties of Pyrene Based Fluorescent Hemicurcuminoid and their BF2 Complexes -Spectroscopic and DFT Studies.

Authors:  Ankush B More; Nagaiyan Sekar
Journal:  J Fluoresc       Date:  2017-05-26       Impact factor: 2.217

2.  Density functional studies on photophysical properties and chemical reactivities of the triarylboranes: effect of the constraint of planarity.

Authors:  Jun-Ling Jin; Hai-Bin Li; Tian Lu; Yu-Ai Duan; Yun Geng; Yong Wu; Zhong-Min Su
Journal:  J Mol Model       Date:  2013-05-25       Impact factor: 1.810

3.  Excitation spectra of dibenzoborole containing pi-electron systems: controlling the electronic spectra by changing the p(pi)-pi* conjugation.

Authors:  Kanchana S Thanthiriwatte; Steven R Gwaltney
Journal:  J Phys Chem A       Date:  2006-02-23       Impact factor: 2.781

4.  Direct functionalization of C-H bonds by electrophilic anions.

Authors:  Jonas Warneke; Martin Mayer; Markus Rohdenburg; Xin Ma; Judy K Y Liu; Max Grellmann; Sreekanta Debnath; Vladimir A Azov; Edoardo Apra; Robert P Young; Carsten Jenne; Grant E Johnson; Hilkka I Kenttämaa; Knut R Asmis; Julia Laskin
Journal:  Proc Natl Acad Sci U S A       Date:  2020-09-02       Impact factor: 11.205

5.  Donor-acceptor-acceptor-type near-infrared fluorophores that contain dithienophosphole oxide and boryl groups: effect of the boryl group on the nonradiative decay.

Authors:  Yoshiaki Sugihara; Naoto Inai; Masayasu Taki; Thomas Baumgartner; Ryosuke Kawakami; Takashi Saitou; Takeshi Imamura; Takeshi Yanai; Shigehiro Yamaguchi
Journal:  Chem Sci       Date:  2021-03-25       Impact factor: 9.825

6.  Dual-Emissive Difluoroboron Naphthyl-Phenyl β-Diketonate Polylactide Materials: Effects of Heavy Atom Placement and Polymer Molecular Weight.

Authors:  Jelena Samonina-Kosicka; Christopher A DeRosa; William A Morris; Ziyi Fan; Cassandra L Fraser
Journal:  Macromolecules       Date:  2014-05-23       Impact factor: 5.985

7.  Electron transport and nonlinear optical properties of substituted aryldimesityl boranes: a DFT study.

Authors:  Altaf Hussain Pandith; Nasarul Islam
Journal:  PLoS One       Date:  2014-12-05       Impact factor: 3.240

8.  Syntheses, Structures, and Complexation Studies of Tris(organostannyl)methane Derivatives.

Authors:  Anicet Siakam Wendji; Michael Lutter; Lukas M Stratmann; Klaus Jurkschat
Journal:  ChemistryOpen       Date:  2016-10-25       Impact factor: 2.911

9.  Taming the beast: fluoromesityl groups induce a dramatic stability enhancement in boroles.

Authors:  Zuolun Zhang; Robert M Edkins; Martin Haehnel; Marius Wehner; Antonius Eichhorn; Lisa Mailänder; Michael Meier; Johannes Brand; Franziska Brede; Klaus Müller-Buschbaum; Holger Braunschweig; Todd B Marder
Journal:  Chem Sci       Date:  2015-07-13       Impact factor: 9.825

Review 10.  (Hetero)arene-fused boroles: a broad spectrum of applications.

Authors:  Jiang He; Florian Rauch; Maik Finze; Todd B Marder
Journal:  Chem Sci       Date:  2020-11-24       Impact factor: 9.825

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