about
Hidden photoinduced reactivity of the blue fluorescent protein mKalama1Collapse and recovery of green fluorescent protein chromophore emission through topological effects.Optically modulatable blue fluorescent proteins.Chromophore photoreduction in red fluorescent proteins is responsible for bleaching and phototoxicityEffect of Ca²⁺ on the steady-state and time-resolved emission properties of the genetically encoded fluorescent sensor CatchERKillerOrange, a Genetically Encoded Photosensitizer Activated by Blue and Green Light.Green fluorescent protein with anionic tryptophan-based chromophore and long fluorescence lifetime.Excited-State Proton Transfer in Chiral Environments: Photoracemization of BINOLs.Topochemistry and photomechanical effects in crystals of green fluorescent protein-like chromophores: effects of hydrogen bonding and crystal packing.Novel uses of fluorescent proteins.Fluorescence imaging using synthetic GFP chromophores.Hydroxycruciforms: amine-responsive fluorophores.Unsymmetrical cruciforms.Excited state proton transfer in reverse micelles.Microcrystals with enhanced emission prepared from hydrophobic analogues of the green fluorescent protein chromophore via reprecipitation.Excited-state proton transfer reactions of 10-hydroxycamptothecin.Activation and tuning of green fluorescent protein chromophore emission by alkyl substituent-mediated crystal packing.Excited-State Dynamics of Oxyluciferin in Firefly Luciferase.6-hydroxyquinoline-N-oxides: a new class of "super" photoacids.Excited-state proton transfer in gas-expanded liquids: the roles of pressure and composition in supercritical CO2/methanol mixtures.Meta and para effects in the ultrafast excited-state dynamics of the green fluorescent protein chromophores.Probing the decay coordinate of the green fluorescent protein: arrest of cis-trans isomerization by the protein significantly narrows the fluorescence spectra.Spectral and redox properties of the GFP synthetic chromophores as a function of pH in buffered media.Conjugates of Benzoxazole and GFP Chromophore with Aggregation-Induced Enhanced Emission: Influence of the Chain Length on the Formation of Particles and on the Dye Uptake by Living Cells.pH-Sensitive fluorophores from locked GFP chromophores by a non-alternant analogue of the photochemical meta effect.Red-shifted fluorescent aminated derivatives of a conformationally locked GFP chromophore.A synthetic approach to GFP chromophore analogs from 3-azidocinnamates. Role of methyl rotors in chromophore photophysics.Conformationally locked chromophores as models of excited-state proton transfer in fluorescent proteins.Reactive oxygen species in photochemistry of the red fluorescent protein "Killer Red".Photoinduced dynamics of oxyluciferin analogues: unusual enol "super"photoacidity and evidence for keto-enol isomerization.Self-assembled benzophenone bis-urea macrocycles facilitate selective oxidations by singlet oxygen.Thermochemiluminescent peroxide crystalsReversible attachment of perylenediimide fluorophore to glass surfaces via strong hydrogen-bondingHydroxy-cruciformsHydroxydialkylamino cruciforms: amphoteric materials with unique photophysical propertiesCompetition and interplay of various intermolecular interactions in ultrafast excited-state proton and electron transfer reactionsTurning on Solid-State Fluorescence with LightDesigning redder and brighter fluorophores by synergistic tuning of ground and excited statesIsolation of biologically active compounds from mangrove sediments
P50
Q27700035-C65DAC2F-A50D-4DC7-B4F9-87B66238D1C1Q30155490-B36A95A0-74CC-4682-84C1-7A41D44D4C39Q31141068-ACDC9FC3-8CBF-4F32-88E7-547835648CC6Q33567093-EB3A9A32-C4F7-4587-B082-22734016471BQ35087826-B528FB00-BEAC-41F4-AB07-C053767ED20BQ35872052-E8C941D8-565E-446C-94E4-447EAF62A467Q36210675-84916ADE-1C3B-4BAE-9882-73785A5E93F2Q37374615-ACEA894D-64B8-488F-9C49-9732F417980BQ38486801-C147A3BB-89D1-428D-8DEA-F3E21DCBE4DDQ38507017-C7FB4C5F-939A-49F0-A342-8E0D26F10160Q38539215-6C7ED927-119E-46D3-ACDC-A4DD5DDAD97DQ42162779-695D6353-0EFB-4795-8D14-207562296ECCQ43254937-FFEF64B1-5B15-4488-A5D0-5F7BE8C2A529Q44032967-00327944-3F43-49C3-AA8C-76E8EB4D8C4BQ44912382-E5DA6E33-39E9-4AC3-8520-FDDD50D0519DQ45082693-44C2C371-B75D-4C37-90D2-0E0B62943974Q46165047-8759A85F-89B1-4966-8E18-E22EAA20BEF4Q46442652-1ECC7DBD-032B-4D39-9C13-961971A0A75BQ46532545-7E4BCAED-0788-4D2E-9A60-43CE72A91C04Q46665194-2B11988E-6BBA-45B6-ADDB-EDDD4C52F413Q46758250-4119F0DB-E542-49F5-9AFD-AA417C3A4E2BQ46920317-2F4E72B5-F241-4E75-88D1-C4D87205F58FQ47949116-31D605D9-0264-46C1-84EE-3DF40F009F1DQ50212785-8544AE91-9346-46E0-9042-5BE0A3FA326BQ50218562-483BB549-6D26-4EEC-A586-3E5B72497BAAQ50450334-28E08F29-12D7-4A2D-92F8-D3851F46A976Q50480234-B45AD562-6A2E-4932-BACF-4A2545B8152FQ50501111-D72281D6-E025-4AA0-B466-54C2C62A4189Q50525890-2589DFA4-A251-4429-9183-C17A8D5AAE6BQ52743792-38F800E5-CD85-44D6-9EB7-63C4A0DB8D04Q53714482-262284FB-0145-45DB-AA93-E6C5688DF54DQ64082705-4351709C-D5C0-4F84-8DF5-11F755EE89D0Q80198594-A9FAB937-2A27-4BF0-8338-3E0F24D7951FQ80371488-E74B573C-C180-4089-BB68-1DFEA9E2C0A8Q83460687-4358C9BB-4A9B-416E-9736-E2090E28C034Q85288417-D9C17BE9-1AA4-4C7A-B8D9-399232BC636EQ88944161-4BD97DCC-2BA6-4A65-B518-BB5080922159Q91451588-2C4CDFD9-3D19-46D6-9804-D7B83F427413Q91977374-B20146BF-E500-4C7D-A361-07EC894145BA
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Kirill Michailowitsch Solnzew
@de
Kyril M Solntsev
@ast
Kyril M Solntsev
@es
Kyril M Solntsev
@nl
Kyril M Solntsev
@sl
Kyril Solntsev
@en
Кирилл Михайлович Солнцев
@ru
type
label
Kirill Michailowitsch Solnzew
@de
Kyril M Solntsev
@ast
Kyril M Solntsev
@es
Kyril M Solntsev
@nl
Kyril M Solntsev
@sl
Kyril Solntsev
@en
Кирилл Михайлович Солнцев
@ru
altLabel
Kirill Mikhaylovich Solntsev
@en
Kirill Solntsev
@en
Kirill Solnzew
@de
Kyril M Solntsev
@en
prefLabel
Kirill Michailowitsch Solnzew
@de
Kyril M Solntsev
@ast
Kyril M Solntsev
@es
Kyril M Solntsev
@nl
Kyril M Solntsev
@sl
Kyril Solntsev
@en
Кирилл Михайлович Солнцев
@ru
P106
P21
P31
P496
0000-0002-6855-462X