About: Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More

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scientific article published on 01 May 1999

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1999 (uk) artículu científicu espublizáu en mayu de 1999 (ast) scientific article published on 01 May 1999 (en)
publication date	wds:Q88520937-D626C248-0E5B-4160-9DD4-2E0B11184F73
publication date	1999-05-01 00:00:00Z (xsd:dateTime)
rdfs:label	Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More (en) Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More (nl)
skos:prefLabel	Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More (en) Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More (nl)
name	Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More (en) Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More (nl)
author	wds:Q88520937-1F25C642-29F8-4B08-BF5B-D5F62FA49002 wds:Q88520937-B3797DED-8911-4CF7-9980-05807FE15E94
author	François Diederich Rainer E Martin
title	wds:Q88520937-B179820F-F36E-421E-96CD-1F98BABA6038
title	Linear Monodisperse π-Conjugated Oligomers: Model Compounds for Polymers and More (en)
page(s)	wds:Q88520937-4D0C18B1-AD2A-4BC6-AB6E-55DB967F04BF
page(s)	1350-1377
instance of	wds:Q88520937-23F287C8-3079-4EF2-BF65-BFBB38AFB5EF
instance of	scholarly article
PubMed ID	wds:Q88520937-43647946-4D60-4107-8270-BF318E22A682
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/29711590
PubMed ID	29711590
published in	wds:Q88520937-AA198A45-85AC-41B9-8C98-1B3BCA5C52B0
published in	Angewandte Chemie International Edition
issue	wds:Q88520937-9EB616D1-FA79-4235-910A-AE66450FA02D
volume	wds:Q88520937-01516EA9-C8EE-4E00-B111-82BB19124C0F
issue	10
volume	38
DOI	wds:Q88520937-8AE0FF88-FE10-48AF-84E1-65EF42FEECEF
DOI	http://dx.doi.org/10.1002/(SICI)1521-3773(19990517)38:10%3C1350::AID-ANIE1350%3E3.0.CO;2-6
DOI	10.1002/(SICI)1521-3773(19990517)38:10<1350::AID-ANIE1350>3.0.CO;2-6
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q88520937
is cites work of	Cycloaddition of 1,3-butadiynes: efficient synthesis of carbo- and heterocycles Synthesis of polyynes to model the sp-carbon allotrope carbyne Iterative exponential growth of stereo- and sequence-controlled polymers Theoretical investigations on the geometric and electronic structures of phenylene-acetylene macrocycles Electronic energy transfer and collection in luminescent molecular rods containing ruthenium(II) and osmium(II) 2,2':6',2"-terpyridine complexes linked by thiophene-2,5-diyl spacers Metallo-supramolecular oligo(p-phenylene vinylene)/[60]fullerene architectures: towards functional materials Phosphole-containing pi-conjugated systems: from model molecules to polymer films on electrodes Synthesis of optically active tetrameric melanin intermediates by oxidation of the melanogenic precursor 5,6-dihydroxyindole-2-carboxylic acid under biomimetic conditions The surprising nonlinear optical properties of conjugated polyyne oligomers Theoretical description of the Raman spectrum of a vinylene-bridged quaterthiophene oligomer Through versus cross electron delocalization in polytriacetylene oligomers: a computational analysis Ground and excited states of linked and fused zinc porphyrin dimers: Symmetry adapted cluster (SAC)—configuration interaction (CI) study Directly linked porphyrin arrays Linear, Non-Conjugated Cyclic and Conjugated Cyclic Paraphenylene under Pressure Synthesis of 9,9'-Spirobifluorenes and 4,5-Diaza-9,9'-spirobifluorenes and Their Application as Affinity Materials for Quartz Crystal Microbalances The loss of endgroup effects in long pyridyl-endcapped oligoynes on the way to carbyne Optical gap and fundamental gap of oligoynes and carbyne A facile copper(I)-catalyzed homocoupling of terminal alkynes to 1,3-diynes with diaziridinone under mild conditions Extension of conjugation leading to bathochromic or hypsochromic effects in OPV series Tailoring Colors by O Annulation of Polycyclic Aromatic Hydrocarbons Stereoselective synthesis of substituted all-trans 1,3,5,7-octatetraenes by a modified Ramberg–Bäcklund reaction Comprehensive Photophysical Behaviour of Ethynyl Fluorenes and Ethynyl Anthracenes Investigated by Fast and Ultrafast Time-Resolved Spectroscopy Single-Crystal X-ray Structures of conductive π-Stacking Dimers of Tetrakis(alkylthio)benzene Radical Cations Infrared spectra of two sexithiophenes in neutral and doped states: a theoretical and spectroscopic study Synthesis and Electrochromic Properties of Conducting Polymers Based on Highly Planar 2,7-Disubstituted Xanthene Derivatives Fabrication of ultrathin films with large third-order nonlinear optical properties. Alternative Synthesis and Structures of C-monoacetylenic Phosphaalkenes. First synthesis of meso-substituted pyrrolo[1,2-a]quinoxalinoporphyrins Impact of Local Stiffness on Entropy Driven Microscopic Dynamics of Polythiophene Highly stereocontrolled synthesis of trans-enediynes via carbocupration of fluoroalkylated diynes Linear and Star-Shaped Extended Di- and Tristyrylbenzenes: Synthesis, Characterization and Optical Response to Acid and Metal Ions (E)-1-(4-Bromo-phen-yl)-2-(4-tert-butyl-phen-yl)-1-phenyl-ethene π-Conjugation of two nitronyl nitroxides-attached diarylethenes. An Iterative Approach tocis-Oligodiacetylenes Vibrational study of push–pull chromophores for second-order non-linear optics derived from rigidified thiophene π-conjugating spacers
is cites work of	wds:Q27021578-4B05CE9B-91B6-485D-AC6F-FB3AD0D74DC0 wds:Q30995154-8FC539A8-E2D2-44CC-A8F3-A3836AC04140 wds:Q62568186-4F03544D-2F97-4223-BD31-98CE0AFCEE34 wds:Q81594240-F1E427AE-E98D-48D1-A929-85888A5D7815 wds:Q79243929-ED06A84D-CA71-46E4-BA9C-D1EE4663CDD3 wds:Q90334565-F35E8653-5F3D-4032-A594-3B5FECD9034A wds:Q92799519-6872D78B-772D-471D-8CC8-60B686994D58 wds:Q101476432-4152459B-304D-4502-8AAD-3FB4F40809EC wds:Q37664174-9013AF1E-12C1-414F-A5AF-5BFFA54BACFE wds:Q43784624-9317B2D2-E80C-488B-99F4-3322FAA6585A wds:Q43873346-431CF8DD-3761-4D52-89BC-4272564DFE9E wds:Q56764531-20CFB59C-5589-4CE5-8800-DA50407065EF wds:Q62568192-1A38BB38-98AB-4886-B179-373980C247D2 wds:Q62661374-13723293-689E-4432-955B-04CD7324E468 wds:Q92884192-D2ECE678-B854-42E7-8DC2-FDA0C1E65CCB wds:Q80367651-304FE671-5193-402A-BCC2-393292BF1259 wds:Q96609590-174682ED-3D8C-40BB-8D13-1AD7E6C13F23 wds:Q38993380-085C107F-DFE0-499D-A3D5-AAD5E80ED051 wds:Q37086347-A6249A9E-EFD3-4621-85DA-BB3923C1BDB3 wds:Q42025465-B2A29DA2-8D27-42D4-8C82-8F686EF2BD45 wds:Q42705687-8D6FB295-8D9C-4921-BD6D-34CB84B08225 wds:Q75306571-1A46F037-0042-4F8E-A6AE-9C4A3E040498 wds:Q99616632-F6035CF7-9993-4DBB-9027-85050172549E wds:Q37396193-61821B8B-3A44-4008-B68B-3C0186865698 wds:Q59456061-2ECAB451-394C-4DBB-87A6-8ACEEFDCDAFE wds:Q79315122-8E1F04A7-ADB8-4F11-9340-EC97991926C5 wds:Q90706128-9541DAA6-1172-400B-AA7D-ED2EF4855631 wds:Q62075532-62373E09-B3A6-4B06-AADD-6EBB410473FC wds:Q41999518-D074EB3E-0C2D-4EDC-893A-D159C903A202

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