about
Synthesis and Characterization of New Organometallic Benzo[b]thiophene Derivatives with Potential Antitumor PropertiesThe key role of coligands in novel ruthenium(II)-cyclopentadienyl bipyridine derivatives: Ranging from non-cytotoxic to highly cytotoxic compounds.pH-Switchability and Second-Order Nonlinear Optical Properties of Monocyclopentadienylruthenium(II)/iron(II) Tetrazoles/Tetrazolates: Synthesis, Characterization, and Time-Dependent Density Functional Theory Calculations.Important cytotoxicity of novel iron(II) cyclopentadienyl complexes with imidazole based ligands.Studies of the Antiproliferative Activity of Ruthenium (II) Cyclopentadienyl-Derived Complexes with Nitrogen Coordinated Ligands.Novel ruthenium methylcyclopentadienyl complex bearing a bipyridine perfluorinated ligand shows strong activity towards colorectal cancer cells.Enzymatic biotransformation of the azo dye Sudan Orange G with bacterial CotA-laccase.DNA interaction and cytotoxicity studies of new ruthenium(II) cyclopentadienyl derivative complexes containing heteroaromatic ligandsSynthesis, structural characterization and leishmanicidal activity evaluation of ferrocenyl N-heterocyclic compoundsDensity functional theory calculations on η5-monocyclopentadienylnitrilecobalt complexes concerning their second-order nonlinear optical propertiesNew iron(II) cyclopentadienyl derivative complexes: Synthesis and antitumor activity against human leukemia cancer cellsη6-(2-phenoxyethanol) ruthenium(II)-complexes of 2,2′-bipyridine and its derivatives: Solution speciation and kinetic behaviourRu( p-cymene) Compounds as Effective and Selective Anticancer Candidates with No Toxicity in VivoNew polydentate Ru(III)-Salan complexes: Synthesis, characterization, anti-tumour activity and interaction with human serum proteinsA Sustainable Synthesis of Asymmetric Phenazines and Phenoxazinones Mediated by CotA-LaccaseEngineering a Bacterial DyP-Type Peroxidase for Enhanced Oxidation of Lignin-Related Phenolics at Alkaline pHEco-friendly synthesis of indo dyes mediated by a bacterial laccaseAn enzymatic route to a benzocarbazole framework using bacterial CotA laccaseBacterial Enzymes and Multi-enzymatic Systems for Cleaning-up Dyes from the EnvironmentTowards the rational biosynthesis of substituted phenazines and phenoxazinones by laccasesLaccase-Catalysed Homocoupling of Primary Aromatic Amines towards the Biosynthesis of DyesMethyl syringate: An efficient phenolic mediator for bacterial and fungal laccasesOn the Mechanism of Biotransformation of the Anthraquinonic Dye Acid Blue 62 by LaccasesSynthesis of Azobenzene Dyes Mediated by CotA LaccaseMono(η5-cyclopentadienyl)metal(II) Complexes with Thienyl Acetylide Chromophores: Synthesis, Electrochemical Studies, and First HyperpolarizabilitiesBenzo[c]thiophene Chromophores Linked to Cationic Fe and Ru Derivatives for NLO Materials: Synthesis Characterization and Quadratic HyperpolarizabilitiesSynthesis of new Fe(II) and Ru(II) η5-monocyclopentadienyl compounds showing significant second order NLO propertiesSynthesis and structural characterization of new piano-stool ruthenium(II) complexes bearing 1-butylimidazole heteroaromatic ligandEvaluation of intermolecular interactions in thioxanthone derivatives: substituent effect on crystal diversityInsights into the mechanism of azo and anthraquinonic dyes biotransformation by the Bacillus subtilis laccaseSynthesis and electrochemical studies of η5-monocyclopentadienylruthenium(II) complexes with substituted thiophene nitrile ligands. Crystal structure of [Ru(η5-C5H5)(dppe)(NC{SC4H2}2NO2)][PF6]Synthesis and structural characterization of ruthenium(II) and iron(II) complexes containing 1,2-di-(2-thienyl)-ethene derived ligands as chromophoresSynthesis of organometallic Ru(II) and Fe(II) complexes containing fused rings hemi-helical ligands as chromophores. Evaluation of non-linear optical properties by HRSCompromise between conjugation length and charge-transfer in nonlinear optical η5-monocyclopentadienyliron(II) complexes with substituted oligo-thiophene nitrile ligands: Synthesis, electrochemical studies and first hyperpolarizabilitiesMechanisms of enzymatic degradation of azo and anthraquinone dyes by bacterial CotA-laccaseSynthesis, Characterisation and Molecular Hyperpolarisabilities of Pseudo-Octahedral Hydrido(nitrile)iron(II) Complexes for Nonlinear Optics: X-ray Structure of [Fe(H)(dppe)2(4-NCC6H4NO2)][PF6]·CH2Cl2The effect of counter-ions on the supramolecular arrangement of (benzonitrile)[1,2-bis(diphenylphosphino)ethane](η5-cyclopentadienyl)iron(II) cationsA supramolecular zigzag chain of organometallic dipoles mediated by PF6−anionsSynthesis, characterization and crystal structure of the bimetallic cyano-bridged [(η5-C5H5)(PPh3)2Ru(μ-CN)Ru(PPh3)2(η5-C5H5)][PF6]High first hyperpolarizability and perfectly aligned crystal packing for an organometallic compound [Fe( η 5 -C 5 H 5 )((R)–PROPHOS)( p -NCC 6 H 4 NO 2 )][PF 6 ]·CH 2 Cl 2
P50
Q28468269-F1F6002A-BDA6-476D-AF60-71B72295D769Q30978989-8E52291D-B435-45E9-8EDC-300700EC5841Q38676307-5496AC8D-A641-468D-BA76-F98A67356D67Q39101770-CDB76D98-2EDB-4661-A8CB-AB9407AB9669Q42109757-71677995-E0CD-486C-9543-3D831D3E6236Q47373109-E022677F-E6BC-4A48-91F4-AAAA3151D527Q51866178-666CA0A4-16D6-42D1-97A1-92A66B3AF61CQ57185326-7DBB2D3A-30AA-423B-B1C6-DBF8F5124392Q57674300-7B9AFE10-F7F0-4316-9A2A-DD1DD268C3D0Q57747234-9ED4CFF6-220F-401F-AFCD-81AB7C40F075Q58478819-272A0236-382A-4EF8-AB24-00F6B3FE8308Q58572071-EB1A842C-73BD-4CA3-A62E-024D8466A39DQ58610435-FECAB956-87FA-4A6D-B3D5-03E70EF1463DQ59082617-F14ACA51-FBBD-41DB-A890-B39E4F0EBB01Q59592082-13624D0C-8935-4A85-9438-D4EF5E567C2FQ59592084-A44235F5-C16B-423F-82C0-46EFB8AF8FFBQ59592086-7A6439C7-E45C-41A0-BA50-6DB95B693279Q59592087-8EA8F368-42B9-45B7-B26F-1936B0794E84Q59592089-76B6A6DB-9C35-4114-90FF-F0E887C2809AQ59592094-D66CFDF0-4F11-4E94-902E-B71E6F859511Q59592096-53619C0F-E574-4967-8314-A6C6A0767F33Q59592099-270E1E58-B406-48D6-B4AE-07A98FA72922Q59592107-844005ED-B8BF-4283-B7EA-D67F7F82BF3CQ59592121-0E2C0CFB-5313-49F6-A727-BA13D8183083Q59592122-F83B6C9D-B675-4EAF-B473-F5C8F4D70273Q59592123-4DE185E0-48CA-439D-A710-03EF834A3385Q59592132-2414B0A2-7D10-423B-A657-CD3F92291A92Q59592134-B1E163E2-926D-4AB6-8582-9347DEF30BA6Q59592135-1B12DE07-E939-4481-8DCF-080554FBEE50Q59592138-D615385B-79D2-4F7C-A69C-15A2A6B8CA42Q59592140-F19E2DE1-F12F-41DD-97B5-BB15D3C82062Q59592142-12B0FA1F-9B03-4D3D-A452-51D512E0BCC1Q59592144-BA485CC7-E167-47E1-A64B-D349A78329ACQ59592145-9B93F3BC-F837-4588-9A04-AAA0C6B3DC0BQ59592146-49F901C7-66D8-4596-9807-EF2AEFD77FCCQ59592147-9ACE05E9-DD90-4B08-AF5D-79547D56BA71Q59592148-84540B5A-83B0-4AA2-B418-5179DBE93734Q59592149-C1737D31-5A44-43E2-8FF7-ACB26C5B3EEAQ59592150-4E39F5E9-ACE7-4BAA-BCD7-033F2D96DE5BQ59592153-D5C1225E-7AAA-4972-9E0D-24F5D2C42DB1
P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0002-8200-6910
@en
name
Maria Paula Robalo
@ast
Maria Paula Robalo
@en
Maria Paula Robalo
@es
Maria Paula Robalo
@nl
type
label
Maria Paula Robalo
@ast
Maria Paula Robalo
@en
Maria Paula Robalo
@es
Maria Paula Robalo
@nl
prefLabel
Maria Paula Robalo
@ast
Maria Paula Robalo
@en
Maria Paula Robalo
@es
Maria Paula Robalo
@nl
P106
P1153
9269662100
P21
P31
P496
0000-0002-8200-6910