about
Oxacalix[n](het)arenes.Unraveling the fluorescence features of individual corrole NH tautomers.Combined experimental-theoretical NMR study on 2,5-bis(5-aryl-3-hexylthiophen-2-yl)-thiazolo[5,4-d]thiazole derivatives for printable electronics.The Influence of Conjugated Polymer Side Chain Manipulation on the Efficiency and Stability of Polymer Solar Cells.A three-step synthetic approach to asymmetrically functionalized 4H-cyclopenta[2,1-b:3,4-b']dithiophenes.Synthetic, structural, and photophysical exploration of meso-pyrimidinyl-substituted AB2-corroles.meso-Pyrimidinyl-substituted A2B- and A3-corroles.Actuated conformational switching in a single crystal of a homodithiacalix[4]arene.Corrole NH tautomers: spectral features and individual protonation.Origin of the Individual Basicity of Corrole NH-Tautomers: A Quantum Chemical Study on Molecular Structure and Dynamics, Kinetics, and Thermodynamics.Absorption and Fluorescence Features of an Amphiphilic meso-Pyrimidinylcorrole: Experimental Study and Quantum Chemical Calculations.meso-Dichloropyrimidinyl substituted expanded porphyrins.Quantum chemical insights into the dependence of porphyrin basicity on the meso-aryl substituents: thermodynamics, buckling, reaction sites and molecular flexibility.Conjugated Polymer Nanoparticles for Bioimaging.Disentangling overlapping high-field EPR spectra of organic radicals: Identification of light-induced polarons in the record fullerene-free solar cell blend PBDB-T:ITIC.Molecular structures and absorption spectra assignment of corrole NH tautomers.High-Permittivity Conjugated Polyelectrolyte Interlayers for High-Performance Bulk Heterojunction Organic Solar Cells.Homodiselenacalix[4]arenes: Molecules with Unique Channelled Crystal Structures.Continuous Flow Polymer Synthesis toward Reproducible Large-Scale Production for Efficient Bulk Heterojunction Organic Solar Cells.TOF-SIMS investigation of degradation pathways occurring in a variety of organic photovoltaic devices--the ISOS-3 inter-laboratory collaboration.Organic phototransistors using poly(3-hexylthiophene) nanofibres.Porphyrin-functionalized dendrimers: synthesis and application as recyclable photocatalysts in a nanofiltration membrane reactor.Elucidating Batch-to-Batch Variation Caused by Homocoupled Side Products in Solution-Processable Organic Solar CellsEffect of molecular weight on morphology and photovoltaic properties in P3HT:PCBM solar cellsToward bulk heterojunction polymer solar cells with thermally stable active layer morphologyInfluence of fullerene photodimerization on the PCBM crystallization in polymer: Fullerene bulk heterojunctions under thermal stressSynthesis of Multi(metallo)porphyrin Dendrimers through Nucleophilic Aromatic Substitution onmeso-Pyrimidinyl Substituted PorphyrinsCombustion deposition of MoO3 films: from fundamentals to OPV applicationsExpanding the Scope of Diamond Surface Chemistry: Stille and Sonogashira Cross-Coupling ReactionsWorldwide outdoor round robin study of organic photovoltaic devices and modulesOn the stability of a variety of organic photovoltaic devices by IPCE and in situ IPCE analyses – the ISOS-3 inter-laboratory collaborationAmphiphilic N-methylimidazole-functionalized diblock copolythiophenesRegioregular Polythiophene-Porphyrin Supramolecular Copolymers for Optoelectronic ApplicationsSelf-assembled conjugated polyelectrolyte–surfactant complexes as efficient cathode interlayer materials for bulk heterojunction organic solar cellsElectronic structure of positive and negative polarons in functionalized dithienylthiazolo[5,4-d]thiazoles: a combined EPR and DFT studyCharge transfer in the weak driving force limit in blends of MDMO-PPV and dithienylthiazolo[5,4-d]thiazoles towards organic photovoltaics with high VOCImproved thermal stability of bulk heterojunctions based on side-chain functionalized poly(3-alkylthiophene) copolymers and PCBMImidazolium-substituted ionic (co)polythiophenes: Compositional influence on solution behavior and thermal propertiesBranched and linear A2–D–A1–D–A2 isoindigo-based solution-processable small molecules for organic field-effect transistors and solar cellsLinear and propeller-like fluoro-isoindigo based donor–acceptor small molecules for organic solar cells
P50
Q37307542-09EBD05B-DC27-4D64-AB84-0DFD6900EED9Q39551559-100F6602-9145-4A50-AE12-6854F2B74FC1Q39628503-4CAE4276-1C97-45B1-84A3-155C1ACDF65EQ41999790-1F0C1240-8158-4BD4-A0F7-33CB1D6602CFQ42868619-90BD27F6-00FE-4DD3-B3A0-144535689469Q43098723-D1CB8A62-9085-419E-87AD-26BCB1DA7F31Q43151888-EDC73EE7-7808-44FF-A80A-B7677B769A6EQ44727918-AD113D3A-4C5B-420F-8EB4-16728340CF3DQ44868968-113CD2AA-6D5C-40E1-B613-FDB7987A9B7EQ46118896-B92A8435-0D56-47E7-8D92-2F092D12AFA9Q46236708-B5E972CE-26CC-4F96-877E-8D83C9F28E2FQ46496083-629DBAB5-87F8-42C9-8983-EC0CF399A15AQ46730692-B61917D6-A9A1-41C5-BE6E-4B8293D269D8Q47138211-BFA0FA61-094D-4391-8910-720A4CE2BBBAQ49791418-DF01DA0F-23F2-4B42-949D-DD9A149068A3Q50226218-23638404-0AB3-4F59-8752-AB7129D09387Q51481987-7E1953C6-64B7-4C04-89F2-5DDEB0AECD34Q51617243-5280C5E7-35D4-4EF4-8B42-E361BEE61773Q51713856-9C29F241-704B-4FF3-84D4-9C30583F2782Q53150336-2ED03DBE-4EC3-454C-8B19-0B4C8A2C7CE4Q53336508-3FCB8E72-051B-4CD4-9B39-5D110B59AF22Q53845582-14D94EE4-D0E0-400E-95BD-307A1783722EQ57563083-44A1596F-A99A-4704-AAAC-4A80168B768DQ57563142-0D32ABB4-0E30-45E8-B133-637730A4A523Q57563191-AEEDFFB6-670E-442F-BB2D-70DC69EC3639Q57563205-9B7196AE-4041-4CD1-B8FC-72F5DA6CCB6CQ57711324-4C8B9FB9-DE91-4B8F-B7F9-2AE71C55B132Q57961720-CBF925E5-B6DB-47C1-8123-0B69F97107D7Q58003173-7A93C647-245D-4FAA-B971-7FCB06B892BCQ58028443-CD09061A-D171-4913-BCC8-7C7C7794920CQ58028488-39FFF8DD-9E89-4C5E-B693-8EB676ED4B38Q58384162-DB31B23D-067A-476D-A77B-0073871B48C1Q59396068-7CA9702B-039B-4967-B140-28C75DDC0643Q59396079-3C2EB746-FF88-4B22-86A7-8CD35C4C26D7Q59612168-C28427ED-A97E-4B21-9A28-DB10769EC867Q59612233-F8E6672B-A027-4813-8F61-2AE243C59324Q60150486-B235BDF5-3CB8-48F6-A33D-BCE14D5ADE84Q63971175-A82F9170-A209-4D21-B96F-EB5175D278F3Q64217787-A1A76CE6-7B4F-47EE-9BCD-621DFC29573EQ64217803-2697AAF6-AA57-4760-B50C-5D607AB2D5B3
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Wouter Maes
@ast
Wouter Maes
@en
Wouter Maes
@es
Wouter Maes
@nl
Wouter Maes
@sl
type
label
Wouter Maes
@ast
Wouter Maes
@en
Wouter Maes
@es
Wouter Maes
@nl
Wouter Maes
@sl
prefLabel
Wouter Maes
@ast
Wouter Maes
@en
Wouter Maes
@es
Wouter Maes
@nl
Wouter Maes
@sl
P106
P21
P31
P496
0000-0001-7883-3393