about
The chemistry of fluorescent bodipy dyes: versatility unsurpassed.Luminescent materials: locking π-conjugated and heterocyclic ligands with boron(III).Rodlike fluorescent pi-conjugated 3,3'-bipyridazine ligand: optical, electronic, and complexation properties.Boron asymmetry in a BODIPY derivative.Length dependence for intramolecular energy transfer in three- and four-color donor-spacer-acceptor arrays.Improved push-pull-push E-Bodipy fluorophores for two-photon cell-imaging.Cation sensors based on terpyridine-functionalized boradiazaindacene.Convenient and efficient synthesis of functionalized oligopyridine ligands bearing accessory pyrromethene-BF2 fluorophores.Fluorescent boron(III) iminocoumarins (Boricos).BODIPY derivatives as donor materials for bulk heterojunction solar cells.Electronic energy transfer to the S2 level of the acceptor in functionalised boron dipyrromethene dyes.Solid-state gas sensors developed from functional difluoroboradiazaindacene dyes.Pyrromethene dialkynyl borane complexes for "cascatelle" energy transfer and protein labeling.The elusive phosphorescence of pyrromethene-BF2 dyes revealed in new multicomponent species containing Ru(II)-terpyridine subunits.Luminescent excited-state intramolecular proton-transfer (ESIPT) dyes based on 4-alkyne-functionalized [2,2'-bipyridine]-3,3'-diol dyes.Intramolecular energy transfer in pyrene-bodipy molecular dyads and triads.2-(2'-Hydroxyphenyl)benzimidazole and 9,10-phenanthroimidazole chelates and borate complexes: solution- and solid-state emitters.Synthetic routes to fluorescent dyes exhibiting large Stokes shifts.Water-soluble red-emitting distyryl-borondipyrromethene (BODIPY) dyes for biolabeling.Chemistry at boron: synthesis and properties of red to near-IR fluorescent dyes based on boron-substituted diisoindolomethene frameworks.Water-solubilisation and bio-conjugation of a red-emitting BODIPY marker.Tailoring the properties of boron-dipyrromethene dyes with acetylenic functions at the 2,6,8 and 4-B substitution positions.An artificial light-harvesting array constructed from multiple Bodipy dyes.NIR lanthanide luminescence by energy transfer from appended terpyridine-boradiazaindacene dyes.Electronic energy transfer in molecular dyads built around boron-ethyne-substituted subphthalocyanines.Rapid intersystem crossing in closely-spaced but orthogonal molecular dyads.Boron Dipyrromethene Dyes Bearing Ancillary 2,2′:6′,2″-Terpyridine Coordination SitesSynthesis of Indolo[3,2- b]carbazole-Based Boron Complexes with Tunable Photophysical and Electrochemical PropertiesIonic self-assembly of ammonium-based amphiphiles and negatively charged bodipy and porphyrin luminophoresElectron transfer in self-assembled orthogonal structuresSynthesis and photophysical properties of borondipyrromethene dyes bearing aryl substituents at the boron centerUnusual fluorescent monomeric and dimeric dialkynyl dipyrromethene-borane complexesEthynyl-boron subphthalocyanines displaying efficient cascade energy transfer and large Stokes shiftsSynthesis of luminescent 2-(2'-hydroxyphenyl)benzoxazole (HBO) borate complexesIsocyanate-, isothiocyanate-, urea-, and thiourea-substituted boron dipyrromethene dyes as fluorescent probesHighly substituted Bodipy dyes with spectroscopic features sensitive to the environmentWater-soluble BODIPY derivativesA general synthetic route to 3,5-substituted boron dipyrromethenes: applications and propertiesBoron dipyrromethene dyes: a rational avenue for sensing and light emitting devicesCarbonyl derivatives of boradiazaindacene via catalytic CO insertion
P50
Q33311304-E0903754-DA10-46D3-AC0F-CBBC13EDA0C1Q38183801-BD711193-53F3-4064-9AE0-01E4FFC5C2FBQ43111082-D3DCCCFF-0B2C-4592-BE2B-DC9A76C33B3AQ43126496-297EA917-3BEF-4093-84FB-72BB0FD53456Q43276593-DA96FA27-3CF2-436E-921E-ECEFBD28FD28Q43286047-B74515DF-9C98-472F-A311-E0ED4A7D382BQ44547984-767BE400-1FF5-4B0A-A5A0-24310BE50FF2Q44826058-4957A583-D5D2-4E22-B12B-23D4D313AB70Q45845031-E28C8C2C-3E16-4A97-AAAA-A89DD630F2FDQ46084862-B7F233BC-6D06-44B2-A96A-01C4E0AC9B18Q46085897-5B701BE9-750C-4B87-8E75-654B53932684Q46179768-CD315383-FFEB-40E0-B53E-EA8267FDE775Q46509207-84B27A8A-60C1-444B-973E-3A567A66CA5AQ46650718-A30DBB0A-D7C4-46BB-BA2D-A661439336B4Q46682854-D93D348D-338B-49C2-B505-5435FD508CD4Q46712153-27316375-8D6F-4A3D-A4F7-34350931A386Q50232625-CFDD1FF2-1733-4F7E-A70D-FA5A1905A468Q50493006-8151AC3A-3B48-4E29-AB47-A159977E2A2CQ50512006-5D667D22-55B5-4F03-89A1-3338920E7F48Q50539870-38F7ACFB-18C4-4F66-9051-623572AE74E8Q50554536-B1987E71-DF82-49B0-9C28-86C56DFFBA86Q50650366-15E360B6-95CC-4B99-8B8C-8D043C49C6AAQ51797364-2B67A6A2-2DD4-4F26-87A1-7A9A6F2A9D0AQ51943110-0A8BC701-8B74-466B-A546-0E7167B0E5E0Q53360767-A5C9763A-463E-46C1-A2BE-CFE4DC596DF0Q54018234-89219A90-D210-44B0-800C-0511AB2B2A9BQ57329958-E1FF18C8-7062-4B6A-893E-BB82E1A48430Q58617115-440C0D95-3BA4-4274-B76D-915DC7050A35Q79635888-98326C08-59B9-4EAF-8B50-E22C214EFD95Q79806481-9B9D9071-3367-446D-B692-9DF92C304577Q80040865-37507544-E898-4D74-B81B-5AC9A08CBCCBQ80302060-E0F2FBF5-525C-4DB4-AFDE-74874853EA2EQ82257169-AF668C5F-E067-45DA-8C2A-9D199C8FC4B5Q82998261-B3C7738C-C51C-4412-B4BE-A1BE999FE0F4Q83111643-13D19C46-3EEB-403F-8C95-E381E03288DCQ83228111-01E6945A-DBF2-4410-93FD-0D9D4EDBEC59Q83687053-4414E3C9-5835-4466-A827-661BC3C2F87FQ83872953-979549FE-6A97-48EC-81F6-EEEA93351861Q83920040-2A8265B7-659F-404D-AD55-7683820F8769Q84057023-059C402F-20CE-44D9-A29E-FF279D4A2905
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Gilles Ulrich
@ast
Gilles Ulrich
@en
Gilles Ulrich
@es
Gilles Ulrich
@nl
Gilles Ulrich
@sl
type
label
Gilles Ulrich
@ast
Gilles Ulrich
@en
Gilles Ulrich
@es
Gilles Ulrich
@nl
Gilles Ulrich
@sl
prefLabel
Gilles Ulrich
@ast
Gilles Ulrich
@en
Gilles Ulrich
@es
Gilles Ulrich
@nl
Gilles Ulrich
@sl
P1053
Q-6710-2016
P106
P1153
7006833452
P21
P31
P3829
P496
0000-0002-6980-6091