About: Mário Calvete

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Portuguese chemist

Attributes	Values
rdf:type	Item
description	scheikundige (nl) portugiesischer Chemiker (de) químicu portugués (ast) Portugali keemik (et) Portuguese chemist (en) chimist portughez (ro) chimiste portugais (fr) kimist portugez (sq) químic portuguès (ca) químico portugués (gl) כימאי פורטוגזי (he) كيميائي برتغالي (ar) পর্তুগিজ রসায়নবিদ (bn) químico portugués (es)
rdfs:label	Mário Calvete (de) Mário Calvete (en) Mário Calvete (es) Mário Calvete (pt) Mário Calvete (pt-br) Mário J. F. Calvete (nl)
skos:prefLabel	Mário Calvete (de) Mário Calvete (en) Mário Calvete (es) Mário Calvete (pt) Mário Calvete (pt-br) Mário J. F. Calvete (nl)
name	Mário Calvete (de) Mário Calvete (en) Mário Calvete (es) Mário Calvete (pt) Mário Calvete (pt-br) Mário J. F. Calvete (nl)
Scopus author ID	wds:Q58655181-43FE7450-7405-4A67-9180-C78126CECF7F
Scopus author ID	9242660700
given name	wds:Q58655181-133BB562-1A4B-4F33-8767-D5E2FE8A0BEA
given name	Mário
instance of	wds:Q58655181-3AD3F820-30B4-49EB-B5CE-01222F87FF6A
instance of	Homo sapiens
skos:altLabel	Mário J. F. Calvete (de) Mário J. F. Calvete (en)
occupation	wds:Q58655181-2765AC12-A580-4C8E-8380-9B275660B2CF
employer	wds:Q58655181-31848B1C-BE7F-4951-9FC5-DB2F99B050BE
place of birth	wds:Q58655181-2960771f-467e-6672-e70c-df45f2d7cb9c
sex or gender	wds:Q58655181-B58CE17D-29DD-4DD2-9B46-44A0658DEFCD
VIAF ID	wds:Q58655181-5E21CEA4-5484-4F2B-A7DC-C8603B798766
GND ID	wds:Q58655181-93a5e651-4769-5e37-91c4-8e774dc83fb8
country of citizenship	wds:Q58655181-05B54DFE-FE4D-4DCE-ACA2-90C17824D87A
date of birth	wds:Q58655181-cc9d5194-431e-6578-09aa-7888a9956264
educated at	wds:Q58655181-020FA01B-B80A-450F-9B5A-9801DB34BD58
WorldCat Identities ID (superseded)	wds:Q58655181-6BEC2C1F-AE4C-4F40-952D-CB4F6DE19D70
VIAF ID	http://viaf.org/viaf/10906320
GND ID	https://d-nb.info/gnd/12874328X
occupation	chemist
employer	University of Coimbra
place of birth	Figueira da Foz
sex or gender	male
VIAF ID	10906320
GND ID	12874328X
country of citizenship	Portugal
date of birth	1975-01-01 00:00:00Z (xsd:dateTime)
educated at	University of Tübingen
WorldCat Identities ID (superseded)	viaf-10906320
ORCID iD	wds:Q58655181-D3985188-2C6A-425B-AFFC-72C992C4A674
ORCID iD	https://orcid.org/0000-0003-2094-4781
ORCID iD	0000-0003-2094-4781
ResearcherID	wds:Q58655181-F1A4CC79-0E5E-41E4-B6D5-938828BBE6B0
Publons author ID	wds:Q58655181-105DCCE5-2E26-44E3-ADC4-F65AFACF3D4D
ResearcherID	D-5547-2012
Publons author ID	975999
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58655181
is author of	A new glycosidation method through nitrite displacement on substituted nitrobenzenes Tetrabrominated lead naphthalocyanine for optical power limiting. Nonlinear Optical Materials for the Smart Filtering of Optical Radiation 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. 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 units The quest for biocompatible phthalocyanines for molecular imaging: Photophysics, relaxometry and cytotoxicity studies Synthesis of binaphthyl based phosphine and phosphite ligands. Photophysics and nonlinear optical properties of tetra- and octabrominated silicon naphthalocyanines Phthalocyanine Labels for Near-Infrared Fluorescence Imaging of Solid Tumors Indium phthalocyanines with different axial ligands: a study of the influence of the structure on the photophysics and optical limiting properties. Hybrid Metalloporphyrin Magnetic Nanoparticles as Catalysts for Sequential Transformation of Alkenes and CO2 into Cyclic Carbonates Synthesis of new metalloporphyrin triads: efficient and versatile tripod optical sensor for the detection of amines A biocompatible redox MRI probe based on a Mn(ii)/Mn(iii) porphyrin Photoacoustic generation of intense and broadband ultrasound pulses with functionalized carbon nanotubes A recyclable hybrid manganese(III) porphyrin magnetic catalyst for selective olefin epoxidation using molecular oxygen Bioinspired-Metalloporphyrin Magnetic Nanocomposite as a Reusable Catalyst for Synthesis of Diastereomeric (-)-Isopulegol Epoxide: Anticancer Activity Against Human Osteosarcoma Cells (MG-63) Biologically Inspired and Magnetically Recoverable Copper Porphyrinic Catalysts: A Greener Approach for Oxidation of Hydrocarbons with Molecular Oxygen Photoinactivation of microorganisms with sub-micromolar concentrations of imidazolium metallophthalocyanine salts A Cost-Efficient Method for Unsymmetrical Meso-Aryl Porphyrin Synthesis Using NaY Zeolite as an Inorganic Acid Catalyst. Conjugating biomaterials with photosensitizers: advances and perspectives for photodynamic antimicrobial chemotherapy
is author of	wds:Q48296863-0079C72A-D1F3-4AC9-87D8-A221802186C6 wds:Q38778852-F85122D2-2CC2-47A0-AC6E-39C38269049E wds:Q63386060-8FD494AD-4341-47F5-9E18-88F896EE749A wds:Q84700555-4F8B4D23-F3EF-46D4-9A97-DC8778E83C3F wds:Q91675872-CDB4D122-11EA-4945-9AF2-3C0A2F7D7534 wds:Q100520168-4918D6E6-DCED-4D0E-B5F4-971B743B38DB

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