about
Hydrogen-bonded semiconducting pigments for air-stable field-effect transistors.Aryl 5-substitution of a phenyl-pyridine based ligand as a viable way to influence the opto-electronic properties of bis-cyclometalated Ir(III) heteroleptic complexes.Tetracoordinated Bis-phenanthroline Copper-Complex Couple as Efficient Redox Mediators for Dye Solar Cells."Darker-than-black" PbS quantum dots: enhancing optical absorption of colloidal semiconductor nanocrystals via short conjugated ligands.Rational Design of Molecular Hole-Transporting Materials for Perovskite Solar Cells: Direct versus Inverted Device Configurations.A versatile synthesis for new 9,10-bis(4-alkoxyphenyl)-2,7-diiodophenanthrenes: useful precursors for conjugated polymers.Heterogeneous optochemical VOC sensing layers selected by ESI-mass spectrometry.Epindolidiones-Versatile and Stable Hydrogen-Bonded Pigments for Organic Field-Effect Transistors and Light-Emitting DiodesMorphological characterization of poly(phenylacetylene) nanospheres prepared by homogeneous and heterogeneous catalysisMolecular Tailoring of Phenothiazine-Based Hole-Transporting Materials for High-Performing Perovskite Solar CellsMolecular engineering of largely π-extended metal-free sensitizers containing benzothiadiazole units: Approaching 10% efficiency dye-sensitized solar cells using iodine-based electrolytesBeneficial Role of a Bulky Donor Moiety in π-Extended Organic Dyes for Mesoscopic TiO2 Sensitized Solar CellsSustainability of Organic Dye-Sensitized Solar Cells: The Role of Chemical SynthesisEnhancing Dye-Sensitized Solar Cell Performances by Molecular Engineering: Highly Efficient π-Extended Organic SensitizersPhotovoltachromic Device with a Micropatterned Bifunctional Counter ElectrodeAnchoring stability and photovoltaic properties of new D(-π-A)2 dyes for dye-sensitized solar cell applicationsThe suzuki-heck polymerization as a tool for the straightforward obtainment of poly(fluorenylene-vinylene) sensitizers for dye-sensitized solar cellsPtCl(PHCy2){(PCy2O)2H}: a hydrogen bonded phosphinito complex obtained by direct reaction of molecular oxygen with a terminal phosphido complexElectronic supplementary information (ESI) available: Fig. S1: ESI-MS positive spectrum of 2. Fig. S2: 1H NSynthesis and Carbonylation of Platinum(II) Organometallic Complexes with Bis(phosphanyl) Monosulfides− Crystal Structures of [κ2P,S-{Ph2CH2P(S)Ph2}Pt(CH3)(Cl)] and [κP,μ-κS-{Ph2CH2CH2P(S)Ph2}Pt-(CH3)]2[BF4]2Asymmetric allylic alkylation using a polymer-supported palladium catalyst in the presence of chiral ligandsSynthesis, characterisation and catalytic activity of Pd(II) and Ni(II) complexes with new cyclic α-diphenylphosphino-ketoimines. Crystal structure of 2,6-diisopropyl-N-(2-diphenylphosphino-cyclopentylidene)aniline and of 2,6-diisopropyl-N-(2-diphenSynthesis of Phosphido-Bridged Phosphinito Platinum(I) Complexes by Reaction of cis-PtCl2(PHCy2)2 with Oxygenated Bases - Crystal Structure of [(PCy2OMe)Pt(μ-PCy2)]2(Pt-Pt)Bio-sorbable, liquid electrolyte gated thin-film transistor based on a solution-processed zinc oxide layerMonodispersed molecular donors for bulk hetero-junction solar cells: from molecular properties to device performancesIodopropyl-branched polysiloxane gel electrolytes with improved ionic conductivity upon cross-linkingThe Dynamic Organic/Inorganic Interface of Colloidal PbS Quantum DotsExploring the surface chemistry of cesium lead halide perovskite nanocrystals
P50
Q34317546-F2B26918-1A38-4621-A804-D56B3446A9B3Q45213883-49CB12F0-6BF4-4E07-87AE-848CD7744888Q46544215-7F51ABD4-37F2-4BEA-BAB3-4AB05DCAEC29Q46788700-941D2446-736C-4E82-B100-8C26B6074AF3Q47964059-66F26A87-6E8E-4BF8-B3AE-CC3FDE6C7A00Q50956386-4D6A000B-F85F-4DF8-9E81-4A8983B980C0Q51174874-4F7D7DFA-1077-4BB0-9A32-6355A13C4C7AQ57502068-1A570D45-7600-48A8-8C36-862DC995FA64Q57642964-1390CC79-4A44-4239-B9E1-55C54A29E464Q57696607-D90528C9-0AB4-4721-9F4E-4BB5F83E5A12Q58311435-FA7A2AE2-26E4-49E0-9B9D-5B557E217C28Q58311461-97763A84-C6DC-465F-9360-C9A7710F19FBQ58311474-8601118E-30FC-40B1-9692-0069D181C56DQ58311494-2421503C-14DC-4006-B16B-4E9F0719DA1BQ58311518-52E5FD16-3B32-474F-B135-77CD50311286Q58311535-72C137FC-F3E9-422B-865A-D224AEAFB5EAQ58311605-695D2184-FA13-419F-8551-951D5D49E3C9Q60238297-2582D1FB-0D56-4B66-BB5A-F5BAA18B69B5Q60238301-3989D18E-DD20-4B9B-82A5-E63263C61353Q60403279-F641CA1A-305B-474D-8F44-F0ABBF468483Q62598112-4C54E9C9-1CD1-4B70-BE1E-BF3EB9AA92E2Q63374075-4862036F-E9C3-4E05-AE12-E01F245645F9Q63456313-05CB8D9C-D3A4-45CB-A7D2-6350647D8A48Q84619822-F8DE777F-A2B1-47DD-A760-638B80EE1B1EQ85649936-F925E1CF-A3CA-40CF-B9E7-E4C10778F5BBQ89107466-DCCD78F8-5DEF-4216-89CE-7D9959D2B2FDQ90659551-23E57EF8-BAE0-4D42-A052-E024C30B46AD
P50
description
researcher ORCID ID = 0000-0003-2953-0809
@en
wetenschapper
@nl
name
Gian Paolo Suranna
@ast
Gian Paolo Suranna
@en
Gian Paolo Suranna
@es
Gian Paolo Suranna
@nl
type
label
Gian Paolo Suranna
@ast
Gian Paolo Suranna
@en
Gian Paolo Suranna
@es
Gian Paolo Suranna
@nl
prefLabel
Gian Paolo Suranna
@ast
Gian Paolo Suranna
@en
Gian Paolo Suranna
@es
Gian Paolo Suranna
@nl
P106
P1153
6701768479
P21
P31
P496
0000-0003-2953-0809