Trivalent boron as an acceptor in donor-pi-acceptor-type compounds for single- and two-photon excited fluorescence.
about
Intravital microscopy as a tool to study drug delivery in preclinical studies.Water-Soluble Triarylborane Chromophores for One- and Two-Photon Excited Fluorescence Imaging of Mitochondria in Cells.Functionalization of phosphorescent emitters and their host materials by main-group elements for phosphorescent organic light-emitting devices.Lighting the Way to See Inside Two-Photon Absorption Materials: Structure-Property Relationship and Biological Imaging.Recent developments in and perspectives on three-coordinate boron materials: a bright future.Convenient methods for preparing pi-conjugated linkers as building blocks for modular chemistry.Optical and electronic properties of air-stable organoboron compounds with strongly electron-accepting bis(fluoromesityl)boryl groups.Excitation spectra of dibenzoborole containing pi-electron systems: controlling the electronic spectra by changing the p(pi)-pi* conjugation.Experimental and theoretical studies on organic D-π-A systems containing three-coordinate boron moieties as both π-donor and π-acceptor.Direct Introduction of a Dimesitylboryl Group Using Base-Mediated Substitution of Aryl Halides with Silyldimesitylborane.Triarylborane-Based Materials for OLED Applications.Diazaborolyl-boryl push-pull systems with ethynylene-arylene bridges as 'turn-on' fluoride sensors.Triarylborane substituted naphthalimide as a fluoride and cyanide ion sensor.Solvatochromism and fluoride sensing of thienyl-containing benzodiazaboroles.D-π-A triarylboron compounds with tunable push-pull character achieved by modification of both the donor and acceptor moieties.Novel high performance asymmetrical squaraines for small molecule organic solar cells with a high open circuit voltage of 1.12 V.Advantage of the N-alkylation strategy for retaining the molecular planarity for oligothiophene/imidazole/1,10-phenanthroline-based heterocyclic semiconducting and fluorescent compounds.Experimental and theoretical studies of quadrupolar oligothiophene-cored chromophores containing dimesitylboryl moieties as π-accepting end-groups: syntheses, structures, fluorescence, and one- and two-photon absorption.Investigation of two-photon absorption behavior in symmetrical acceptor-pi-acceptor derivatives with dimesitylboryl end-groups. Evidence of new engineering routes for TPA/transparency trade-off optimization.Truxene-cored π-expanded triarylborane dyes as single- and two-photon fluorescent probes for fluoride.Energy redistribution dynamics in triarylamine-triarylborane containing hexaarylbenzenes.Access to new Janus head ligands: linking sulfur diimides and phosphanes for hemilabile tripodal scorpionatesDFT/TDDFT Investigation of the Modulation of Photochromic Properties in an Organoboron-Based Diarylethene by Fluoride Ions
P2860
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P2860
Trivalent boron as an acceptor in donor-pi-acceptor-type compounds for single- and two-photon excited fluorescence.
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Trivalent boron as an acceptor ...... o-photon excited fluorescence.
@ast
Trivalent boron as an acceptor ...... o-photon excited fluorescence.
@en
type
label
Trivalent boron as an acceptor ...... o-photon excited fluorescence.
@ast
Trivalent boron as an acceptor ...... o-photon excited fluorescence.
@en
prefLabel
Trivalent boron as an acceptor ...... o-photon excited fluorescence.
@ast
Trivalent boron as an acceptor ...... o-photon excited fluorescence.
@en
P2093
P356
P1476
Trivalent boron as an acceptor ...... wo-photon excited fluorescence
@en
P2093
P304
P356
10.1002/CHEM.200304833
P407
P50
P577
2003-10-01T00:00:00Z