About: 4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials

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

About: 4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials Goto Sponge NotDistinct Permalink

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

article by Michael Benstead et al published May 2011 in Tetrahedron

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2011 (uk) article scientifique publié en 2011 (fr) im Mai 2011 veröffentlichter wissenschaftlicher Artikel (de) article by Michael Benstead et al published May 2011 in Tetrahedron (en)
publication date	wds:Q57361245-2B8D2775-B9C8-45DB-915D-5DAD036BB65E
publication date	2011-05-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q57361245-44B12420-4F37-45AB-BD1E-9EDE409C537F
cites work	Advances in the chemistry of dipyrrins and their complexes
author name string	wds:Q57361245-21999CF4-24D8-47ED-B488-2D56EFBB21BA wds:Q57361245-49C31667-1D43-48CB-B5AF-14A7FD05E9E2 wds:Q57361245-5E3A2E24-ABBC-47BE-85A1-6FE9157277CC
author name string	Michael Benstead Georg H. Mehl Ross W. Boyle
rdfs:label	4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials (en) 4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials (nl)
skos:prefLabel	4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials (en) 4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials (nl)
name	4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials (en) 4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials (nl)
title	wds:Q57361245-8EEB9275-0C4B-4A76-885F-B504863769EE
title	4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacenes (BODIPYs) as components of novel light active materials (en)
page(s)	wds:Q57361245-8E7E447C-3A75-4247-BA44-4E49239A815B
page(s)	3573-3601
instance of	wds:Q57361245-38BED28B-5F8C-4F10-AB24-E9967C6B405D
instance of	scholarly article
published in	wds:Q57361245-AB7CD6ED-5FA2-4C49-B990-805DAEFB6E5A
published in	Tetrahedron
issue	wds:Q57361245-7F6BC28B-9FE7-4143-82C9-F12E7E517375
volume	wds:Q57361245-35133E46-DAFA-4E21-8935-8F88FB0A7DFA
issue	20
volume	67
number of pages	wds:Q57361245-21C4BD42-BB95-4D99-911E-345A0F13ACF9
number of pages	29 (xsd:decimal)
DOI	wds:Q57361245-3A7D817C-F802-48C5-9234-E3DEFB9357BF
DOI	http://dx.doi.org/10.1016/J.TET.2011.03.028
DOI	10.1016/J.TET.2011.03.028
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57361245
is cites work of	Structural modification strategies for the rational design of red/NIR region BODIPYs Fluorescent sensors based on BODIPY derivatives for aluminium ion recognition: an experimental and theoretical study Coumarin-BODIPY hybrids by heteroatom linkage: versatile, tunable and photostable dye lasers for UV irradiation N-BODIPYs Come into Play: Smart Dyes for Photonic Materials Push-pull flexibly-bridged bis(haloBODIPYs): solvent and spacer switchable red emission. Second-order nonlinear polarizability of ferrocene-BODIPY donor-acceptor adducts. Quantifying charge redistribution in the excited state Synthesis, computational modeling, and properties of benzo-appended BODIPYs. Radical C-H arylation of the BODIPY core with aryldiazonium salts: synthesis of highly fluorescent red-shifted dyes Calculations of BODIPY dyes in the ground and excited states using the M06-2X and PBE0 functionals Antimicrobial activity of a quaternized BODIPY against Staphylococcus strains Synthesis, Structure, and Optical Studies of Donor-Acceptor-Type Near-Infrared (NIR) Aza-Boron-Dipyrromethene (BODIPY) Dyes. Highly Efficient Solid-State Near-infrared Organic Light-Emitting Diodes incorporating A-D-A Dyes based on α,β-unsubstituted "BODIPY" Moieties Effect of the substitution position (2, 3 or 8) on the spectroscopic and photophysical properties of BODIPY dyes with a phenyl, styryl or phenylethynyl group Light-harvesting with panchromatically absorbing BODIPY–porphyrazine conjugates to power electron transfer in supramolecular donor–acceptor ensembles Polymers and the p-block elements Activation of BODIPY fluorescence by the photoinduced dealkylation of a pyridinium quencher A photoswitchable fluorophore for the real-time monitoring of dynamic events in living organisms Halogenated boron-dipyrromethenes: synthesis, properties and applications New 2,6-distyryl-substituted BODIPY isomers: synthesis, photophysical properties, and theoretical calculations Modulation of ICT probability in bi(polyarene)-based O-BODIPYs: towards the development of low-cost bright arene-BODIPY dyads. 3,5-Bis(acetaldehyde) substituted BODIPY. Donor-acceptor, ferrocenyl substituted BODIPYs with marvelous supramolecular interactions. Synergetic Effect in Triplet-Triplet Annihilation Upconversion: Highly Efficient Multi-Chromophore Emitter Sulfur-bridged BODIPY DYEmers Synthesis and Photochemical Properties of 2,3;5,6-bis(cyclohexano)-BODIPY. A highly selective turn-on fluorescent sensor for Cu(II) based on an NSe2 chelating moiety and its application in living cell imaging Conjugated BODIPY DYEmers by metathesis reactions. Polycatenar unsymmetrical β-diketonate ligands as a useful tool to induce columnar mesomorphism on highly luminescent boron difluoride complexes Light-Harvesting Antenna and Proton-Activated Photodynamic Effect of a Novel BODIPY-Fullerene C60 Dyad as Potential Antimicrobial Agent Novel Alkoxy-Substituted Dipyrrins and Near-IR BODIPY Dyes-Preparation and Photophysical Properties UV-vis spectroscopy of the coupling products of the palladium-catalyzed C-H arylation of the BODIPY core. Boroquinol Complexes with Fused Extended Aromatic Backbones: Synthesis and Optical Properties. Deuteration and tautomeric reactivity of the 1-methyl functionality of free-base dipyrrins. A Modular Class of Fluorescent Difluoroboranes: Synthesis, Structure, Optical Properties, Theoretical Calculations and Applications for Biological Imaging. Introducing asymmetry in tetradentate azadipyrromethene chromophores: a systematic study of the impact on electronic and photophysical properties. Biological Evaluation of Dipyrromethanes in Cancer Cell Lines: Antiproliferative and Pro-apoptotic Properties. Robust synthesis of F-BODIPYs. Prodigiosenes conjugated to tamoxifen and estradiol. BODIPY dyes with thienyl- and dithienylthio-substituents - synthesis, redox and fluorescent properties. Synthesis and polymorphism evaluation of the 3,5-bis(decyloxy)benzaldehyde Synthesis and characterization of pyrrolyldipyrrin F-BODIPYs.
is cites work of	wds:Q36362087-0D509462-79BB-449A-90A7-5FD4E032EE1C wds:Q39043433-D6F0F2E2-BED8-4048-93ED-723BC356212E wds:Q40810116-05D792FB-5FA3-41D6-92F5-2D0AA501BAC2 wds:Q48599858-1D330771-F860-4D2A-BFAE-59C538FF3168 wds:Q48346142-A3D76906-F64A-4359-B917-356D21E4D1AF wds:Q57528834-566F1EE9-7A5C-4259-89F0-8F55D5E4C9A9 wds:Q37318208-AA55F6D4-9B85-4FDB-9ABC-148F260ACAC0 wds:Q38707127-D7564A47-9433-4FAD-BAD4-43AE99D6052C wds:Q35570301-F26E6864-4190-42E7-8649-200E495566E9 wds:Q44110822-60E9EFB9-6DA8-4150-9B88-A32E4A932A3B wds:Q46168326-C6F620BA-F475-44DE-832E-C33863C64A1C wds:Q46771445-952005A0-9D95-4DC8-805A-555FECCA8DAC wds:Q42266984-FC2F8379-CFC6-4FFF-B400-BB9341E58923 wds:Q54040786-8423C292-7346-483D-8037-E415D0D86684 wds:Q50122954-C0B9B773-5584-4E32-BDC6-3510FF7ED0E7 wds:Q57615963-89BAA2CE-B48E-4AA3-B217-5B10D126C0C8 wds:Q92999302-7492DE71-510C-4D5F-87FA-71D5FBFA18C5 wds:Q38320805-3CCB9FD4-D3D0-408A-9F66-2EE215E044B2 wds:Q46091143-BD363CBA-BEAB-479C-B958-07B7064411AB

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, 171 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software