about
Lewis acidity enhancement of triarylboranes via peripheral decoration with cationic groups.Structural and electrochemical investigations of the high fluoride affinity of sterically hindered 1,8-bis(boryl)naphthalenes.Chemical reduction and dimerization of 1-chloro-2,3,4,5-tetraphenylborole.A di-substituted boron dication and its hydride-induced transformation to an NHC-stabilized borabenzene.1,2-Migration of N-Diarylboryl Imidazol-2-ylidene through Intermolecular Radical Process.Cyanide ion complexation by a cationic borane.Fluoride ion capture from water with a cationic boraneA 9-borylated acridinyl radicalStructural changes accompanying the stepwise population of a B-C pi bondPlatinum substituted borolesSynthesis and structure of a carbene-stabilized pi-boryl anionFluoride ion recognition by chelating and cationic boranesThe pentaphenylborole-2,6-lutidine adduct: a system with unusual thermochromic and photochromic propertiesNHC-stabilized 1-hydro-1H-borole and its nondegenerate sigmatropic isomersSynthesis, structure, and reactivity of borole-functionalized ferrocenesThe reduction chemistry of ferrocenylboroleTriphenylene-based tris-N-heterocyclic stannylenesA spiroborate-based anionic bis-N-heterocyclic carbeneOligo(borolyl)benzenes--synthesis and propertiesRedox chemistry of a hydroxyphenyl-substituted borane"Mr. Boron", an Inorganic Chemistry Icon, Turns 90PSb+P Ligand: Platform for a Stibenium to Transition-Metal InteractionDestabilizing Character of a π-Conjugated Boron Center in Bisphenol RadicalsSuperior Stability and Emission Quantum Yield (23% ± 3%) of Single-Layer 2D Tin Perovskite TEA2 SnI4 via Thiocyanate PassivationHarnessing Dielectric Confinement on Tin Perovskites to Achieve Emission Quantum Yield up to 21
P50
Q33394318-2E1EEB9B-EB37-4416-A945-AF5A92242F93Q39345697-ECA09F31-FB36-4E69-B3DF-4C099E274A45Q42908182-8C113966-F558-4217-BCAA-2495B104C50CQ46312530-B2915D33-E10A-41B1-BDFF-EA68DF1338C8Q46319303-55A0CF76-C9A0-4C1C-943F-C9122F8F983FQ46778995-17A36BD2-E955-4BF5-8470-BB6A804467C5Q79318879-DDFE54D6-C6EA-4C56-B0B6-198F436B0400Q80068427-DDA4509C-28CB-48F8-B540-F44D9F7ED7ECQ80752468-10796B21-40A1-415B-8560-F76C7F50A48DQ82671835-ACBC8CB4-C42A-47AF-A70D-3FEC0158B6BAQ82911345-06EA0CED-1C7A-4E3F-9B72-4960B66699DBQ83180666-DC94ED4A-CFDD-433E-A14E-42B67358575CQ83569125-955D212F-13A7-4AD9-B016-4CF1BFD439ECQ83824601-29D3AC6B-4012-4D8F-AB6F-379A4B9D2427Q84781227-53612FD3-BA52-4FD1-B60A-ED9C251EA982Q85185885-3199A60F-C1C1-4152-AF7E-8BD5AE1A8DD0Q87015166-27925690-CBBA-4FD9-A49A-A9680A5BEA7BQ87043493-F512B91C-7107-4656-870B-92E2C0329297Q87389884-2A53423D-410C-4ACF-93F6-BB76947B1D87Q87783897-A3709C74-3881-4C87-9320-B4E97E904CF9Q90083415-F2B1D37A-389A-44C3-A856-662429F5DA2FQ90474859-D9F18A2F-42A9-42B2-8CF0-6DED4CC91055Q91280786-0700C92E-1917-47B8-8CB8-8FA9F11DDC33Q92072412-4E524F8C-21E0-4EF0-9D03-A3F67E62263AQ93058720-20EA33FA-40AE-4C66-800A-E0C13F59A717
P50
description
researcher ORCID ID = 0000-0001-7201-0943
@en
wetenschapper
@nl
name
Ching-Wen Chiu
@ast
Ching-Wen Chiu
@en
Ching-Wen Chiu
@es
Ching-Wen Chiu
@nl
type
label
Ching-Wen Chiu
@ast
Ching-Wen Chiu
@en
Ching-Wen Chiu
@es
Ching-Wen Chiu
@nl
prefLabel
Ching-Wen Chiu
@ast
Ching-Wen Chiu
@en
Ching-Wen Chiu
@es
Ching-Wen Chiu
@nl
P31
P496
0000-0001-7201-0943