Results 31 to 40 of about 7,389 (151)

Specific Position of Halogen in Crystalline TADF Scintillators Enables Efficient Triplet Harvesting Through Vibrational Modulation of Spin–Orbit Coupling

open access: yesAdvanced Materials, EarlyView.
Specific ortho‐halogenation transforms crystalline TADF emitters into efficient organic scintillators. Fluorine reduces the effective singlet–triplet separation, while chlorine combines near‐degenerate excited states with vibrational modulation of spin–orbit coupling.
Illia E. Serdiuk   +8 more
wiley   +1 more source

Site-selective chlorination of pyrrolic heterocycles by flavin dependent enzyme PrnC

open access: yesCommunications Chemistry
Halogenation of pyrrole requires strong electrophilic reagents and often leads to undesired polyhalogenated products. Biocatalytic halogenation is a highly attractive approach given its chemoselectivity and benign reaction conditions.
GuangRong Peh   +14 more
doaj   +1 more source

Semi‐Telechelic Polymers from Mechanochemical C─C Bond Activation

open access: yesAdvanced Science, 2023
Unstrained C─C bond activation is attained in homopolymers through mechanochemical bond scission followed by functionalization to yield mostly semi‐telechelic polymer chains.
Rony Schwarz, Charles E. Diesendruck
doaj   +1 more source

A Kinetic–Energetic Bottleneck of Charge‐Transfer Injection Governs Energy Loss in Organic Solar Cells

open access: yesAdvanced Energy Materials, EarlyView.
Kinetic–energetic projection of time‐resolved photoluminescence reveals that charge‐transfer injection acts as a universal bottleneck in organic solar cells. A physics‐constrained Bayesian framework identifies an emergent effective CT injection rate governing the trade‐off between charge generation and nonradiative energy loss.
Rong Wang   +16 more
wiley   +1 more source

Amine and Titanium (IV) Chloride, Boron (III) Chloride or Zirconium (IV) Chloride-Promoted Baylis-Hillman Reactions

open access: yesMolecules, 2001
The Baylis-Hillman reactions of various aryl aldehydes with methyl vinyl ketone at temperatures below -20oC using Lewis acids such as titanium (IV) chloride, boron (III) chloride or zirconium (IV) chloride in the presence of a catalytic amount of ...
Shi-Cong Cui, Jian-Kang Jiang, Min Shi
doaj   +1 more source

A New Method of Halogenation of Aromatic Compounds [PDF]

open access: yesمجلة جامعة الانبار للعلوم الصرفة, 2012
: A halogenation of eleven aromatic compounds using a new method for iodination of activated aromatic compounds is presented. The reaction of one mole of aromatic compound with a mixture of one mole Potassium iodide and two moles Potassium sulfate in the
Marwan M. Farhan
doaj   +1 more source

Electrophilic Reactions of 7-(Trifluoromethyl)-2,3-dihydro- 1H-pyrrolizine: a Way Towards New Building Blocks

open access: yesЖурнал органічної та фармацевтичної хімії, 2023
Aim. To synthesize new fluoro-containing building blocks for medicinal chemistry purposes using electrophilic reactions of 7-(trifluoromethyl)-2,3-dihydro-1H-pyrrolizine. Results and discussion.
Anton A. Klipkov, Igor I. Gerus
doaj   +1 more source

Oxidation of Iodine to Dihaloiodate(I) Salts of Amines With Hydrogen Peroxides and Their Crystal Structures

open access: yesFrontiers in Chemistry, 2022
Herein we report a general preparation of dihaloiodate salts of heterocyclic amines (tertiary and quaternary) with sterically accessible and hindered nitrogen atom.
Griša Grigorij Prinčič   +3 more
doaj   +1 more source

Fine‐Tuning the Photovoltaic Performance of Organic Solar Cells by Collaborative Optimization of Structural Isomerism and Halogen Atom

open access: yesAdvanced Energy & Sustainability Research, 2022
Fused‐ring acceptors based on an electron‐deficient core, such as Y6, have become a successful strategy in bulk heterojunction (BHJ) organic solar cells (OSCs) for high power conversion efficiencies (PCEs).
Zhe Li   +4 more
doaj   +1 more source

Unified Synthesis of Unconventional α‐Polyhalogenated Amines Through Hydroaminoalkylation

open access: yesAngewandte Chemie International Edition, EarlyView.
A unified, redox‐neutral method that transforms alkenes and alkynes into α‐polyhalomethyl amines using stable hemiaminal reagents is reported. This approach enables access to CF3, CF2H, CF2Cl, and CFClH motifs, expanding halogenated amine space with broad substrate scope, functional group tolerance, and applicability to late‐stage modification of drug ...
Angela K. Hofmeister   +9 more
wiley   +1 more source

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