An Azide-Substituted Triarylborane: A Key Compound for the Facile Synthesis of Fluorescent Triarylboranes Bearing Triazole Moieties as Connectable π-Conjugated System Linkages

D−π–A Triarylboranes as Reversible Fluorescent Probes for CO2 and Temperature

(2019) Hai-Jun Li et al.   ORGANIC LETTERS

Self-Assembly of a Highly Emissive Pure Organic Imine-Based Stack for Electroluminescence and Cell Imaging

(2019) Xujun Zheng et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Structurally Constrained Boron-, Nitrogen-, Silicon-, and Phosphorus-Centered Polycyclic π-Conjugated Systems

(2019) Masato Hirai et al.   CHEMICAL REVIEWS

2,2′-Diamino-6,6′-diboryl-1,1′-binaphthyl: A Versatile Building Block for Temperature-Dependent Dual Fluorescence and Switchable Circularly Polarized Luminescence

(2019) Zuo-Bang Sun et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

p-π Conjugated Polymers Based on Stable Triarylborane with n-Type Behavior in Optoelectronic Devices

(2018) Bin Meng et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Di-(2-picolyl)-N- (2-quinolinylmethyl)amine-Functionalized Triarylboron: Lewis Acidity Enhancement and Fluorogenic Discrimination Between Fluoride and Cyanide in Aqueous Solution

(2018) Mao-Sen Yuan et al.   CHEMISTRY-A EUROPEAN JOURNAL

From Monodisperse Thienyl- and Furylborane Oligomers to Polymers: Modulating the Optical Properties through the Hetarene Ratio

(2018) Artur Lik et al.   CHEMISTRY-A EUROPEAN JOURNAL

Dimesitylboryl-functionalised cyanostilbene derivatives of phenothiazine: distinctive polymorphism-dependent emission and mechanofluorochromism

(2018) C. Arivazhagan et al.   CRYSTENGCOMM

Salen-indium/triarylborane triads: synthesis and ratiometric emission-colour changes by fluoride ion binding

(2018) Sang Woo Kwak et al.   DALTON TRANSACTIONS

Donor−π–Acceptor Type Unsymmetrical Triarylborane-Based Fluorophores: Synthesis, Fluorescence Properties, and Photostability

(2018) Masato Ito et al.   JOURNAL OF ORGANIC CHEMISTRY

Design for a small molecule based chemosensor containing boron and pyridine moieties to detect HF

(2018) Ying Hu et al.   SENSORS AND ACTUATORS B-CHEMICAL

A simple multi-responsive system based on aldehyde functionalized amino-boranes

(2018) Yong-gang Shi et al.   Chemical Science

Triarylboryl-substituted carbazoles as bipolar host materials for efficient green phosphorescent organic light-emitting devices

(2018) Chin-Wei Lu et al.   DYES AND PIGMENTS

Triarylborane-Based Materials for OLED Applications

(2017) Gulsen Turkoglu et al.   MOLECULES

Recent developments in and perspectives on three-coordinate boron materials: a bright future

(2017) Lei Ji et al.   Chemical Science

Greatly Enhanced Fluorescence by Increasing the Structural Rigidity of an Imine: Enantioselective Recognition of 1,2-Cyclohexanediamine by a Chiral Aldehyde

(2016) Yimang Xu et al.   CHEMISTRY-A EUROPEAN JOURNAL

Dimesitylarylborane-based luminescent emitters exhibiting highly-efficient thermally activated delayed fluorescence for organic light-emitting diodes

(2016) Yuichi Kitamoto et al.   ORGANIC ELECTRONICS

A highly twisted triarylborane-based biphenyl as an efficient host for blue and green phosphorescent OLEDs

(2016) Chen Wang et al.   Journal of Materials Chemistry C

Higher fluorescence in platinum(iv) orthometallated complexes of perylene imine compared with their platinum(ii) or palladium(ii) analogues

(2015) J. Emilio Expósito et al.   DALTON TRANSACTIONS

Imine (–CHN–) brings selectivity for silver enhanced fluorescence

(2015) Mainak Ganguly et al.   DALTON TRANSACTIONS

Synthesis and Properties of 2-(Dimesitylboryl)benzylideneamines

(2015) Zureima García-Hernández et al.   ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES

An Azido-BODIPY Probe for Glycosylation: Initiation of Strong Fluorescence upon Triazole Formation

(2014) Jiun-Jie Shie et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Photochemistry of Fluorescent Azobenzenes Substituted with Azulenylpyridine Moiety

(2014) Eugenia Andreea Dragu et al.   MOLECULAR CRYSTALS AND LIQUID CRYSTALS

Light-driven fluorescence enhancement and self-assembled structural evolution of an azobenzene derivative

(2014) Xia Ran et al.   Journal of Materials Chemistry C

Fluorescent azobenzenes and aromatic aldimines featuring an N–B interaction

(2013) Junro Yoshino et al.   DALTON TRANSACTIONS

Synthesis of tris(4-amino-2,6-dimethylphenyl)borane and facile extension of its π-conjugated system by utilizing the reactivity of the amino groups

(2013) Junro Yoshino et al.   TETRAHEDRON LETTERS

Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition

(2012) Stefanie Potratz et al.   Beilstein Journal of Organic Chemistry

Synthesis and Photophysical Properties of Aryl-Substituted 2-Borylbenzaldimines and Their Extended π-Conjugated Congeners

(2012) Benedikt Neue et al.   JOURNAL OF ORGANIC CHEMISTRY

Chemistry on Boranils: An Entry to Functionalized Fluorescent Dyes

(2012) Denis Frath et al.   ORGANIC LETTERS

Triazole: a unique building block for the construction of functional materials

(2011) Michal Juríček et al.   CHEMICAL COMMUNICATIONS

Advances in the Synthesis of Organoborane Polymers for Optical, Electronic, and Sensory Applications

(2010) Frieder Jäkle   CHEMICAL REVIEWS

Fluoride Ion Complexation and Sensing Using Organoboron Compounds

(2010) Casey R. Wade et al.   CHEMICAL REVIEWS

New Photochromic Dithienylethenes through a Click Chemistry Approach

(2010) Oliver Tosic et al.   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Impact of Donor−Acceptor Geometry and Metal Chelation on Photophysical Properties and Applications of Triarylboranes

(2009) Zachary M. Hudson et al.   ACCOUNTS OF CHEMICAL RESEARCH

Fluoride Ion Recognition by Chelating and Cationic Boranes

(2009) Todd W. Hudnall et al.   ACCOUNTS OF CHEMICAL RESEARCH

Cu-Catalyzed Azide−Alkyne Cycloaddition

(2008) Morten Meldal et al.   CHEMICAL REVIEWS

Lewis Acidity Enhancement of Triarylboranes via Peripheral Decoration with Cationic Groups

(2008) Ching-Wen Chiu et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY