Results 11 to 20 of about 10,808 (271)

“Activated Borane” – A Porous Borane Cluster Network [PDF]

open access: yes, 2022
The unprecedented co-thermolysis of nido-decaborane (B10H14) and toluene results in a novel porous material (that we have named “Activated Borane”) containing micropores of 1.0 and 1.5 nm in diameter and a specific surface area of 774 m2 g-1 (Ar, 87 K) that is thermally stable up to 1000 oC.
Daniel Bůžek   +9 more
openaire   +1 more source

A borane laser [PDF]

open access: yesNature Communications, 2015
Emission from electronically excited species forms the basis for an important class of light sources-lasers. So far, commercially available solution-processed blue-emitting laser materials are based on organic compounds or semiconductor nanocrystals that have significant limitations: either low solubility, low chemical- and/or photo-stability and/or ...
Cerdán, L.   +4 more
openaire   +4 more sources

The Synthesis, Characterization, and Fluxional Behavior of a Hydridorhodatetraborane

open access: yesMolecules, 2023
The octahydridotriborate anion plays a crucial role in the field of polyhedral boron chemistry, facilitating the synthesis of higher boranes and the preparation of diverse transition metal complexes.
Fatou Diaw-Ndiaye   +3 more
doaj   +1 more source

Catalytic Dehydrogenation of Amine‐Boranes using Geminal Phosphino‐Boranes [PDF]

open access: yesZeitschrift für anorganische und allgemeine Chemie, 2020
The reaction of the intramolecular frustrated Lewis pair (FLP) tBu2PCH2BPh2 with the amine‐boranes NH3·BH3 and Me2NH·BH3 leads to the formation of the corresponding FLP‐H2 adducts as well as novel five‐membered heterocycles that result from capturing the in situ formed amino‐borane by a second equivalent of FLP.
Boom, D.H.A.   +6 more
openaire   +3 more sources

Dehydroborylation of Terminal Alkynes Using Lithium Aminoborohydrides

open access: yesMolecules, 2023
Dehydrogenative borylation of terminal alkynes has recently emerged as an atom-economical one-step alternative to traditional alkyne borylation methodologies.
P. Veeraraghavan Ramachandran   +1 more
doaj   +1 more source

Boranes in Organic Chemistry 1. О±-Carbonylalkyl- and ОІ-Oxyalkylboranes in Organic Synthesis

open access: yesEurasian Chemico-Technological Journal, 2002
This review is devoted to the synthesis of a-carbonylalkyl- and ОІ-hydroxy-alkyl boranes and their use in organic synthesis. a-Carbonyl-alkylboranes include several heteroatomic compounds, in particular, [1.2.3]-diazaborinines, uracyl boronic acids, and [
V.M. Dembitsky   +2 more
doaj   +1 more source

Novel B(Ar')2(Ar'') hetero-tri(aryl)boranes: a systematic study of Lewis acidity [PDF]

open access: yes, 2016
A series of homo- and hetero-tri(aryl)boranes incorporating pentafluorophenyl, 3,5-bis(trifluoromethyl)phenyl, and pentachlorophenyl groups, four of which are novel species, have been studied as the acidic component of frustrated Lewis pairs for the ...
Ashley   +61 more
core   +2 more sources

Blue Emitting Star-Shaped and Octasilsesquioxane-Based Polyanions Bearing Boron Clusters. Photophysical and Thermal Properties

open access: yesMolecules, 2020
High boron content systems were prepared by the peripheral functionalisation of 1,3,5-triphenylbenzene (TPB) and octavinylsilsesquioxane (OVS) with two different anionic boron clusters: closo-dodecaborate (B12) and cobaltabisdicarbollide (COSAN). TPB was
Justo Cabrera-González   +4 more
doaj   +1 more source

The topological uniqueness of the deltahedra found in the boranes BnHn2− (6≤n≤12) [PDF]

open access: yes, 1990
The deltahedra observed experimentally in the borane anions BnHn2− (6≤n≤12) are the only possible n-vertex deltahedra having only degree 4 and 5 vertices.
Duijvestijn, A.J.W., King, R.B.
core   +2 more sources

Diastereoselective three-component synthesis of beta-amino carbonyl compounds using diazo compounds, boranes, and acyl imines under catalyst-free conditions [PDF]

open access: yes, 2014
Diazo compounds, boranes, and acyl imines undergo a three-component Mannich condensation reaction under catalyst-free conditions to give the anti β-amino carbonyl compounds in high diastereoselectivity.
Luan, Yi   +4 more
core   +1 more source

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