Results 61 to 70 of about 2,463 (211)

Composites and Materials Prepared from Boron Cluster Anions and Carboranes

open access: yes, 2023
Here, we present composites and materials that can be prepared starting with boron hydride cluster compounds (decaborane, decahydro-closo-decaborate and dodecahydro-closo-dodecaborate anions and carboranes).
Igor B. Sivaev   +4 more
core   +1 more source

Synthesis of Polyhedral Borane Cluster Fused Heterocycles via Transition Metal Catalyzed B-H Activation

open access: yesMolecules, 2020
Aromatic heterocycles are ubiquitous building blocks in bioactive natural products, pharmaceutical and agrochemical industries. Accordingly, the carborane-fused heterocycles would be potential candidates in drug discovery, nanomaterials ...
Ke Cao   +7 more
doaj   +1 more source

Hydride Materials for Advanced Electrochemical Energy Storage: Progress and Perspectives

open access: yesEcoEnergy, EarlyView.
Hydrides are emerging as functional materials for low‐carbon electrochemical energy storage. Complex hydrides provide polyanionic electrolyte frameworks for all‐solid‐state, Li–S, and multivalent batteries; hydride ion conductors enable H− transport for emerging hydride‐based cells; and metal hydrides offer established electrode chemistries for Ni–MH ...
Taehyun Kim   +4 more
wiley   +1 more source

o‐Carborane‐based multi‐resonance thermally activated delayed fluorescence emitter exhibits highly efficient and multifunctional electroluminescence

open access: yesFlexMat, EarlyView.
By strategically incorporating boron/nitrogen multi‐resonance (B/N‐MR) core into the o‐carborane unit, perfect exciton utilization can be achieved as well as exhibiting stimuli‐responsive properties. The resulting DBN‐oCb‐based organic light‐emitting diode (OLED) demonstrated an impressive external quantum efficiency of 22.3%, the highest reported for ...
Jiasen Zhang   +8 more
wiley   +1 more source

Forging Unsupported Metal–Boryl Bonds with Icosahedral Carboranes [PDF]

open access: yes, 2016
In contrast to the plethora of metal-catalyzed cross-coupling methods available for the installation of functional groups on aromatic hydrocarbons, a comparable variety of methods are currently not available for icosahedral carboranes, which are boron ...
Liban M. A. Saleh   +7 more
core   +1 more source

Synthesis of new representatives of A3B-type carboranylporphyrins based on meso-tetra(pentafluorophenyl)porphyrin transformations

open access: yesBeilstein Journal of Organic Chemistry
A carboranylporphyrin of A3B-type bearing a single pentafluorophenyl ring was prepared through the regioselective nucleophilic aromatic substitution reaction of the p-fluorine atoms in 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin with 9-mercapto-m ...
Victoria M. Alpatova   +3 more
doaj   +1 more source

Insertion of Carbenes into Deprotonated nido-Undecaborane, B11H13(2-)

open access: yesMolecules, 2019
We have examined the insertion of carbenes carrying leaving groups into the [nido-B11H13]2− dianion to form the [closo-1-CB11H12]− anion. The best procedure uses CF3SiMe3 and LiCl as the source of CF2.
Jacek Pecyna   +2 more
doaj   +1 more source

Analysis of Carbohydrates and Glycoconjugates by Matrix‐Assisted Laser Desorption/Ionization Mass Spectrometry: An Update for 2023–2024

open access: yesMass Spectrometry Reviews, EarlyView.
ABSTRACT The use of MALDI mass spectrometry for the analysis of carbohydrates and glycoconjugates is a well‐established technique and this comprehensive review is the twelfth update of the original article published in 1999 and brings coverage of the literature to the end of 2024.
David J. Harvey
wiley   +1 more source

Competition between Halogen, Hydrogen and Dihydrogen Bonding in Brominated Carboranes [PDF]

open access: yes, 2016
Halogen bonds are a subset of noncovalent interactions with rapidly expanding applications in materials and medicinal chemistry. While halogen bonding is well known in organic compounds, it is new in the field of boron cluster chemistry.
Holub, Josef   +18 more
core   +1 more source

Cu(OTf)2/NBS-Mediated Tandem Reaction of 1‑Cinnamyl Alcohol‑o‑Carboranes via Ring Opening of Oxetane with Arenes: An Alternative Approach for the Synthesis of C‑Alkenyl‑o‑Carboranes

open access: yes, 2022
The Cu­(OTf)2/NBS-mediated tandem reaction of 1-cinnamyl alcohol-o-carboranes for the synthesis of C-alkenyl-o-carboranes has been developed. Mechanism studies demonstrated that the Cu­(OTf)2-promoted ring opening of oxetane with electron-rich arenes as ...
Han-Bo Yang (11541098)   +4 more
core   +1 more source

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