about
Ecofriendly porphyrin synthesis by using water under microwave irradiation.Large two-photon absorption cross sections of hemiporphyrazines in the excited state: the multiphoton absorption process of hemiporphyrazines with different central metals.Synthesis of binaphthyl based phosphine and phosphite ligands.Phthalocyanine Labels for Near-Infrared Fluorescence Imaging of Solid Tumors.Nonlinear Optical Materials for the Smart Filtering of Optical Radiation.Tetrabrominated lead naphthalocyanine for optical power limiting.A Cost-Efficient Method for Unsymmetrical Meso-Aryl Porphyrin Synthesis Using NaY Zeolite as an Inorganic Acid Catalyst.Indium phthalocyanines with different axial ligands: a study of the influence of the structure on the photophysics and optical limiting properties.Size and ability do matter! Influence of acidity and pore size on the synthesis of hindered halogenated meso-phenyl porphyrins catalysed by porous solid oxides.Cost-efficient method for unsymmetrical meso-aryl porphyrins and iron oxide-porphyrin hybrids prepared thereof.Energy transfer from fluorene-based conjugated polyelectrolytes to on-chain and self-assembled porphyrin unitsThe quest for biocompatible phthalocyanines for molecular imaging: Photophysics, relaxometry and cytotoxicity studiesBioinspired-Metalloporphyrin Magnetic Nanocomposite as a Reusable Catalyst for Synthesis of Diastereomeric (-)-Isopulegol Epoxide: Anticancer Activity Against Human Osteosarcoma Cells (MG-63)A new glycosidation method through nitrite displacement on substituted nitrobenzenesPhotophysics and nonlinear optical properties of tetra- and octabrominated silicon naphthalocyaninesSynthesis of new metalloporphyrin triads: efficient and versatile tripod optical sensor for the detection of aminesConjugating biomaterials with photosensitizers: advances and perspectives for photodynamic antimicrobial chemotherapyPhotoinactivation of microorganisms with sub-micromolar concentrations of imidazolium metallophthalocyanine saltsA biocompatible redox MRI probe based on a Mn(ii)/Mn(iii) porphyrin
P50
Q30841846-70582874-2BD4-49BC-BCC7-E6B7D5C94925Q33362719-B7DDDF6F-5AD1-4EA9-BA9A-BEA78FAA8C37Q38115696-3D9604AE-2AEF-434A-AC2D-DF0258E3A441Q38778852-F85122D2-2CC2-47A0-AC6E-39C38269049EQ38785306-E6755FB4-8942-4DE2-B046-F3DED4C58602Q43235881-93E1FAB3-940C-480C-92F4-3198DD44053BQ44078557-ECDCA62B-9C65-4B38-B421-B098C3AFF6EEQ46420897-4EE53216-FEE1-4FD8-9D43-B6619CDCC450Q47178181-F8D6C9E0-A925-4C40-9A33-A6D6725E1CF1Q48296863-0079C72A-D1F3-4AC9-87D8-A221802186C6Q57595700-03C51EBC-BDB6-4544-99C9-C0961A32F305Q61083564-3D612DEA-5AB1-4312-A428-34CC1AB63746Q61455232-CA5C6F29-7171-4A02-A719-0DBDDB6249ABQ79444685-55A8B7D8-B3F8-42E7-B396-BDD3C2F9BE98Q80419847-5FA29D4E-20E4-4CBF-8008-882713DEAD02Q84700555-4F8B4D23-F3EF-46D4-9A97-DC8778E83C3FQ89912562-86A644F7-D229-4E70-8899-43A5364EB0ACQ90668563-5CE207D5-4B71-46D2-BECA-0F14E47284F5Q91675872-CDB4D122-11EA-4945-9AF2-3C0A2F7D7534
P50
description
Portugali keemik
@et
Portuguese chemist
@en
chimist portughez
@ro
chimiste portugais
@fr
kimist portugez
@sq
portugiesischer Chemiker
@de
químic portuguès
@ca
químico portugués
@es
químico portugués
@gl
scheikundige
@nl
name
Mário Calvete
@de
Mário Calvete
@en
Mário Calvete
@es
Mário J. F. Calvete
@nl
type
label
Mário Calvete
@de
Mário Calvete
@en
Mário Calvete
@es
Mário J. F. Calvete
@nl
altLabel
Mário J. F. Calvete
@de
Mário J. F. Calvete
@en
prefLabel
Mário Calvete
@de
Mário Calvete
@en
Mário Calvete
@es
Mário J. F. Calvete
@nl
P214
P227
P106
P1153
9242660700
P21
P214
P227
P31
P496
0000-0003-2094-4781
P569
1975-01-01T00:00:00Z
P7859
viaf-10906320