Results 111 to 120 of about 643,193 (264)

LONG-RANGE CARBON-CARBON COUPLING-CONSTANTS OF 9-LABELED ANTHRACENE-DERIVATIVES

, 1974
MARSHALL JL, IHRIG AM, Miller D. LONG-RANGE CARBON-CARBON COUPLING-CONSTANTS OF 9-LABELED ANTHRACENE-DERIVATIVES. Journal of Magnetic Resonance.
MARSHALL, JL, IHRIG, AM, Miller, David
core   +1 more source

From Data to Dimers: Engineering Acene Derivatives for Photovoltaic Singlet Fission

Chemistry – A European Journal, EarlyView.
Excited‐state energies of acene derivatives are predicted using a ChemBERTa‐based regression model and subsequently used to screen candidates for photovoltaic singlet fission using dimer–monomer benchmarked energetic criteria. Promising candidates are predominantly 5‐ and 6‐fused heteroacenes, which offer enhanced stability and higher triplet energies ...
Alexander J. Cross, Rik R. Tykwinski, J. Terence Blaskovits   +2 more
wiley   +1 more source

Correction: Design of triphenylamine appended anthracene derivatives: electro-polymerization and their electro-chromic behaviour

, 2017
Correction for ‘Design of triphenylamine appended anthracene derivatives: electro-polymerization and their electro-chromic behaviour’ by Dines Chandra Santra et al., RSC Adv., 2016, 6, 81597–81606.
Sanjoy Mondal, Dines Chandra Santra, Sudip Malik   +2 more
core   +1 more source

Synthesis and Structures of Novel Chiral Cyclic Hypervalent Iodine(III) Reagents for Metal‐Free Ligand‐Transfer Reactions

Chemistry – A European Journal, EarlyView.
Several new chiral cyclic hypervalent iodine(III) reagents have been synthesized and characterized. Carbon‐based ligands were successfully installed onto the hypervalent iodine centers, giving thus access to novel chiral cyano‐, trifluoromethyl‐ or alkynyl‐bearing λ3‐iodanes.
Emmanuel Valzer, Jean‐Marc Sotiropoulos, Karinne Miqueu, Laurent Pouységu, Stéphane Quideau   +4 more
wiley   +1 more source

2,6-Bis[4-(p-dihexylaminostyryl)styryl]anthracene Derivatives with Large Two-Photon Cross Sections

, 2016
Anthracene derivatives with a variety of donor−acceptor substituents have been synthesized and shown to exhibit large two-photon cross sections over a wide range of ...
Seung-Joon Jeon (2200927), Chang Ho Kim (244448), Jin Joo Choi (2695213), Seung Kyu Lee (2695216), Bong Rae Cho (1797655), Wen Jun Yang (2338987)   +5 more
core   +1 more source

Cyclization of a 1,8‐Diphenylanthracene by Scholl Reactions to Form Five‐ and Seven‐Membered Ring Embedded Polycyclic Aromatic Hydrocarbons

Chemistry – A European Journal, EarlyView.
Reactions of 10‐mesityl‐1,8‐diphenylanthracene with DDQ/TfOH produced three products via sequential formation of a five‐ or seven‐membered ring. Unexpectedly, the triply cyclized product with a rubicene substructure was formed through cyclization involving 1,2‐methyl shift.
Tatsuhiro Sasaki, Eiji Tsurumaki, Shinji Toyota   +2 more
wiley   +1 more source

Anthracenediylidene derivatives: control of molecular and supramolecular architecture [PDF]

, 2002
In the context of new π-donor molecules, extended tetrathiafulvalenes have been widely studies for their use as components of electronically conductive charge-transfer materials.
Godbert, Nicolas
core  

Halogenated Tryptophans Improve Integrin αVβ6 Affinity of Cyclic RGD Peptides and Provide Handles for Late‐Stage Derivatization

Chemistry – A European Journal, EarlyView.
Lighting up αVβ6: Halotryptophan engineering converts an RGD scaffold into a modular αVβ6 ligand platform, enabling picomolar affinity and late‐stage functionalization. The resulting probes combine high selectivity with fluorescence for FACS and tumor imaging.
Beate Nachtigall, Caroline Brinkmann, Jana Langosch, Anke Nieß, Norbert Sewald   +4 more
wiley   +1 more source

Photoreduction of Anthracene Derivatives

Nippon kagaku zassi, 1968
Jiro OSUGI, Sigeru KUSUHARA, Satoshi HIRAYAMA   +2 more
openaire   +2 more sources

Light upconversion by triplet-triplet anihilation in anthracene derivatives. [PDF]

, 2016
TTA-UC ( upconvertion by triplet- triplet annihilation) process can be preformed by low intensity excitation sources (10mW/cm2). This creates a wide range of applications.
Rimkus, Deividas,
core