Related references
Note: Only part of the references are listed.Fluorescence-based measurement of the Lewis acidities of lanthanide triflates in solution
Paul Demay-Drouhard et al.
CANADIAN JOURNAL OF CHEMISTRY (2022)
Tetrachlorocatecholates of triarylarsines as a novel class of Lewis acids
Akane Chishiro et al.
DALTON TRANSACTIONS (2022)
Phosphorus-Based Catalysis
Changmin Xie et al.
ACS CENTRAL SCIENCE (2021)
Cationic Carbene Analogues: Donor-Free Phosphenium and Arsenium Ions
Marian Olaru et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2021)
Thermoneutral N-H Bond Activation of Ammonia by a Geometrically Constrained Phosphine
Josh Abbenseth et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2021)
Lewis Superacidic Catecholato Phosphonium Ions: Phosphorus-Ligand Cooperative C-H Bond Activation
Daniel Roth et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2021)
The formation of cage phosphoranes and their rearrangements in the reactions of substituted 2-(3-oxo-3-phenyl)ethoxybenzo[d]-1,3,2-dioxaphospholes with perfluorodiacetyl
Vladimir F. Mironov et al.
CHEMICAL COMMUNICATIONS (2021)
Structure-reactivity studies on hypervalent square-pyramidal dithieno[3,2-b:2′,3′-d]phospholes
Nayanthara Asok et al.
DALTON TRANSACTIONS (2021)
Nitrenium Salts in Lewis Acid Catalysis
Meera Mehta et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)
Synthesis of Blue-Luminescent Seven-Membered Phosphorus Heterocycles
Elzbieta Regulska et al.
JOURNAL OF ORGANIC CHEMISTRY (2020)
Molecular Bismuth Cations: Assessment of Soft Lewis Acidity
Jacqueline Ramler et al.
CHEMISTRY-A EUROPEAN JOURNAL (2020)
Lewis acids and bases as molecular dopants for organic semiconductors
Colin R. Bridges et al.
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY (2020)
High Lewis Acidity at Planar, Trivalent, and Neutral Bismuth Centers
Katherine M. Marczenko et al.
ORGANOMETALLICS (2020)
Fluorescent Lewis Adducts: A Practical Guide to Relative Lewis Acidity
Jordan N. Bentley et al.
ORGANOMETALLICS (2020)
A Simple and Effective Method of Determining Lewis Acidity by Using Fluorescence
Joshua R. Gaffen et al.
CHEM (2019)
Strong Enhancement of π-Electron Donor/Acceptor Ability by Complementary DD/AA Hydrogen Bonding
Cheng-Hao Liu et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2019)
Periodicity in Structure, Bonding, and Reactivity for p-Block Complexes of a Geometry Constraining Triamide Ligand
Katherine M. Marczenko et al.
CHEMISTRY-A EUROPEAN JOURNAL (2019)
Synthesis of a Trivalent P-Chloro-Dithienophosphole and Its Reactivity with Organometallic Reagents
Joshua R. Gaffen et al.
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY (2019)
Bis(perchlorocatecholato)silaneA Neutral Silicon Lewis Super Acid
Rezisha Maskey et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2018)
On the reactivity of P-chloro dithieno[3,2-b:2 ',3 '-d]phosphole oxide
Zisu Wang et al.
CANADIAN JOURNAL OF CHEMISTRY (2018)
The global electrophilicity index as a metric for Lewis acidity
Andrew R. Jupp et al.
DALTON TRANSACTIONS (2018)
Exploration of Hypervalent Lewis Acid/Base Interactions in 2-(2′-Thiazolyl)-3-thienylphosphanes
Nicole Grenon et al.
INORGANIC CHEMISTRY (2018)
An Unexpected Step-Conjugated'' Biphosphole via Unique P-P Bond Formation
Zisu Wang et al.
CHEM (2018)
Phosphorus Coordination Chemistry in Catalysis: Air Stable P(III)-Dications as Lewis Acid Catalysts for the Allylation of C-F Bonds
Saurabh S. Chitnis et al.
ORGANOMETALLICS (2018)
Dithienophosphole-Based Phosphinamides with Intriguing Self-Assembly Behavior
Zisu Wang et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)
Phosphorus Lewis acids: emerging reactivity and applications in catalysis
J. M. Bayne et al.
CHEMICAL SOCIETY REVIEWS (2016)
The broadening reach of frustrated Lewis pair chemistry
Douglas W. Stephan
SCIENCE (2016)
β-Hydrogen Elimination Mechanism in the Absence of Low-Lying Acceptor Orbitals in EH2(t-C4H9) (E = N-Bi)
Andreas Stegmueller et al.
INORGANIC CHEMISTRY (2015)
Control of a Chiral Property of a Calix[3]aramide: The Racemization Suppressed by Intramolecular Cyclic. Hydrogen Bonds and DMSO-H2O System-Induced Spontaneous Resolution
Kosuke Katagiri et al.
ORGANIC LETTERS (2015)
Insights on the Design and Electron-Acceptor Properties of Conjugated Organophosphorus Materials
Thomas Baumgartner
ACCOUNTS OF CHEMICAL RESEARCH (2014)
Lewis acidic stiborafluorenes for the fluorescence turn-on sensing of fluoride in drinking water at ppm concentrations
Masato Hirai et al.
CHEMICAL SCIENCE (2014)
Dithieno[3,2-c:2′,3′-e]-2,7-diketophosphepin: A Unique Building Block for Multifunctional π-Conjugated Materials
Xiaoming He et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2013)
Lewis Acidity of Organofluorophosphonium Salts: Hydrodefluorination by a Saturated Acceptor
Christopher B. Caputo et al.
SCIENCE (2013)
Dithieno[3,2-b:2′,3′-d]phospholes: A Look Back at the First Decade
Carlos Romero-Nieto et al.
SYNLETT (2013)
2,2′-Biphospholes: Building Blocks for Tuning the HOMO-LUMO Gap of π-Systems Using Covalent Bonding and Metal Coordination
Hui Chen et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2012)
External-Stimuli Responsive Photophysics and Liquid Crystal Properties of Self-Assembled Phosphole-Lipids
Yi Ren et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
Simple access to the non-oxidizing Lewis superacid PhF -> Al(OR(F))(3) (R(F) = C(CF(3))(3))
Lutz O. Mueller et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2008)
Cationic dithieno[3,2-b:2′,3′-d]phospholes:: A new building block for luminescent, conjugated polyelectrolytes
Stefan Durben et al.
ORGANIC LETTERS (2006)
Highly sensitive sensory materials for fluoride ions based on the dithieno[3,2-b:2′,3′-d]phosphole system
T Neumann et al.
ORGANIC LETTERS (2006)
Novel metal-free Lewis acid catalysis by phosphonium salts through hypervalent interaction
M Terada et al.
TETRAHEDRON (2006)
A critical review of the development of the CIE1931 RGB color-matching functions
AD Broadbent
COLOR RESEARCH AND APPLICATION (2004)
Connecting π-chromophores by σ-P-P bonds:: New type of assemblies exhibiting σ-π-conjugation
C Fave et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2004)
Share Paper
