About: Martin R. Bryce

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Martin R. Bryce Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

chemist

Attributes	Values
rdf:type	Item
description	chemist (en) scheikundige (nl) хімік (uk)
rdfs:label	Martin R. Bryce (en) Martin R. Bryce (es) Martin R. Bryce (nl) Martin R. Bryce (sl) Martin R. Bryce (sq) Martin R. Bryce (ast)
skos:prefLabel	Martin R. Bryce (en) Martin R. Bryce (es) Martin R. Bryce (nl) Martin R. Bryce (sl) Martin R. Bryce (sq) Martin R. Bryce (ast)
name	Martin R. Bryce (en) Martin R. Bryce (es) Martin R. Bryce (nl) Martin R. Bryce (sl) Martin R. Bryce (sq) Martin R. Bryce (ast)
given name	wds:Q53938986-15209586-32B7-49EB-8D82-FC5D1C4A1FD5
given name	Martin
instance of	wds:Q53938986-E16FA2E3-5A4E-4022-A637-E3B2E9592C3E
instance of	Homo sapiens
award received	wds:Q53938986-11d6952c-4124-5e6f-596c-e9569df2cf26 wds:Q53938986-27ea3d04-4c96-3173-a631-75d0a80a4388
award received	Interdisciplinary Prize Bader Prize
skos:altLabel	Martin Bryce (en)
occupation	wds:Q53938986-52EFEED7-0C85-4D95-A58A-AAB8E818B6F8
employer	wds:Q53938986-522850ed-4133-1ea8-9d3d-781a677f0494
sex or gender	wds:Q53938986-D01E9EB0-754D-4171-8E6C-25151D7BCF7A
ISNI	wds:Q53938986-EC08B08A-212D-4570-AC2F-8E68923BB7EB
VIAF ID	wds:Q53938986-128337FD-5E89-4381-A9F2-C6A985DF214C
Bibliothèque nationale de France ID	wds:Q53938986-B66F1352-00FF-40D9-9CFF-DA420BFABBF1
IdRef ID	wds:Q53938986-E7634A93-4BF0-425C-9056-5EB1BED5D974
educated at	wds:Q53938986-3efb428d-4aad-166e-ee85-f943f3b1238a
family name	wds:Q53938986-4BA034B0-07D6-4861-BF93-15ADAC9DCE42
National Library of Israel J9U ID	wds:Q53938986-9D2DCF4F-614B-4E45-BDAA-A25E02EADA00
official website	wds:Q53938986-d5f3c26c-4bb5-3b0d-f208-9a9ed22cadf9
VIAF ID	http://viaf.org/viaf/19785713
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb12512078x#about
IdRef ID	http://www.idref.fr/081099797/id
occupation	chemist
employer	Durham University
sex or gender	male
ISNI	0000000030532279
VIAF ID	19785713
Bibliothèque nationale de France ID	12512078x
IdRef ID	081099797
educated at	York University
family name	Bryce
National Library of Israel J9U ID	987007443395405171
official website	https://www.dur.ac.uk/chemistry/staff/profile/?id=172
ORCID iD	wds:Q53938986-54C68FB9-B21A-4A70-89EB-9491DF221664
ORCID iD	https://orcid.org/0000-0003-2097-7823
ORCID iD	0000-0003-2097-7823
ResearcherID	wds:Q53938986-4d22b06a-4716-fa59-6fd2-3195a888b489
Publons author ID	wds:Q53938986-e7068f62-b915-4639-97f2-9e8986ce8d4f
ResearcherID	I-2356-2012
Publons author ID	2702737
ORKG ID	wds:Q53938986-53a431ba-2e4a-481c-b0a8-97abe00ab8d6
ORKG ID	R141819
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q53938986
is author of	Functionalisation reactions of 2,5-diphenyl-1,3,4-oxadiazoles bearing a terminal ethynyl or butadiynyl substituent: X-ray crystal structures of the products Ethynyl pi-extended 2,5-diphenyl-1,3,4-oxadiazoles and 2-phenyl 5-(2-thienyl)-1,3,4-oxadiazoles: synthesis, X-ray crystal structures and optical properties Electrochromic tetrathiafulvalene derivatives functionalised with 2,5-diaryl-1,3,4-oxadiazole chromophores Quantum interference and heteroaromaticity of para- and meta-linked bridged biphenyl units in single molecular conductance measurements A quantum circuit rule for interference effects in single-molecule electrical junctions. Dipolar stabilization of emissive singlet charge transfer excited states in polyfluorene copolymers Variable contact gap single-molecule conductance determination for a series of conjugated molecular bridges Single-Molecule Conductance of Functionalized Oligoynes: Length Dependence and Junction Evolution Electron Acceptors of the Fluorene Series. 10.1Novel Acceptors Containing Butylsulfanyl, Butylsulfinyl, and Butylsulfonyl Substituents: Synthesis, Cyclic Voltammetry, Charge-Transfer Complexation with Anthracene in Solution, and X-ray Crystal Structu Correlation of breaking forces, conductances and geometries of molecular junctions Identifying diversity in nanoscale electrical break junctions. Electrical conductance of conjugated oligomers at the single molecule level. Unambiguous one-molecule conductance measurements under ambient conditions Recent advances in white organic light-emitting materials and devices (WOLEDs). The first studies of a tetrathiafulvalene-sigma-acceptor molecular rectifier Carbon-rich molecules: synthesis and isolation of aryl/heteroaryl terminal bis(butadiynes) (HC[triple bond]C-C[triple bond]C-Ar-C[triple bond]C-C[triple bond]CH) and their applications in the synthesis of oligo(arylenebutadiynylene) molecular wires Thermally induced defluorination during a mer to fac transformation of a blue-green phosphorescent cyclometalated iridium(III) complex. A biosensor for monitoring formaldehyde using a new lipophilic tetrathiafulvalene-tetracyanoquinodimethane salt and a polyurethane membrane Precision control of single-molecule electrical junctions. Combining high electron affinity and intramolecular charge transfer in 1,3-dithiole-nitrofluorene push-pull diads Triplet harvesting with 100% efficiency by way of thermally activated delayed fluorescence in charge transfer OLED emitters. A study of planar anchor groups for graphene-based single-molecule electronics Single-molecule electrical studies on a 7 nm long molecular wire 5-Formyl-2-furylboronic acid as a versatile bifunctional reagent for the synthesis of pi-extended heteroarylfuran systems 5-Pyrimidylboronic acid and 2-methoxy-5-pyrimidylboronic acid: new heteroarylpyrimidine derivatives via Suzuki cross-coupling reactions Palladium-catalyzed cross-coupling reactions of pyridylboronic acids with heteroaryl halides bearing a primary amine group: synthesis of highly substituted bipyridines and pyrazinopyridines Experimental Evidence for Quantum Interference and Vibrationally Induced Decoherence in Single-Molecule Junctions Oligoyne single molecule wires. Intramolecular charge transfer assisted by conformational changes in the excited state of fluorene-dibenzothiophene-S,S-dioxide co-oligomers. Tuning the intramolecular charge transfer emission from deep blue to green in ambipolar systems based on dibenzothiophene S,S-dioxide by manipulation of conjugation and strength of the electron donor units The interplay of conformation and photophysical properties in deep-blue fluorescent oligomers Synthesis and properties of functionalized oligo(arylene) molecular wires with thiolated termini: competing thiol-Au and nitro-Au assembly Efficient intramolecular charge transfer in oligoyne-linked donor-pi-acceptor molecules Using Guest-Host Interactions To Optimize the Efficiency of TADF OLEDs.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 172 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software