About: Francisco P. dos Santos

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

researcher ORCID ID = 0000-0003-1530-9505

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) researcher ORCID ID = 0000-0003-1530-9505 (en)
rdfs:label	Francisco P. dos Santos (en) Francisco P. dos Santos (es) Francisco P. dos Santos (nl) Francisco P. dos Santos (ast)
skos:prefLabel	Francisco P. dos Santos (en) Francisco P. dos Santos (es) Francisco P. dos Santos (nl) Francisco P. dos Santos (ast)
name	Francisco P. dos Santos (en) Francisco P. dos Santos (es) Francisco P. dos Santos (nl) Francisco P. dos Santos (ast)
Scopus author ID	wds:Q59564513-419498A2-208B-47A4-96BB-705F9AE03B68
Scopus author ID	12809690300
given name	wds:Q59564513-74B8F837-C065-4AD7-9C47-239EC59199F2
given name	Francisco
instance of	wds:Q59564513-E27A2D8B-5B1E-46A6-B4EC-88559350AC34
instance of	Homo sapiens
occupation	wds:Q59564513-56558DC1-96A7-4951-BC5A-C47625E2DE64
employer	wds:Q59564513-87D761E1-C2AE-42F1-95D3-ACD5A1429E97
sex or gender	wds:Q59564513-84E33117-6C9D-488F-AA22-7BE547862278
educated at	wds:Q59564513-394B177E-0BBE-4C1F-A8EF-1E25CA50AEA5
family name	wds:Q59564513-A0AEA7F9-7627-4EC3-8A73-DE3336228D44
occupation	researcher
employer	Federal University of Rio Grande do Sul
sex or gender	male
educated at	University of Campinas
family name	dos Santos
ORCID iD	wds:Q59564513-AE113602-AEC0-41D9-B55C-FCC85A856953
ORCID iD	https://orcid.org/0000-0003-1530-9505
ORCID iD	0000-0003-1530-9505
ResearcherID	wds:Q59564513-BF91E407-7264-481F-B69C-E110107145DD
ResearcherID	C-9537-2015
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59564513
is author of	Intermolecular hydrogen bonds in water@IL supramolecular complexes. Confined water in imidazolium based ionic liquids: a supramolecular guest@host complex case. Carbon Dioxide Capture by Aqueous Ionic Liquid Solutions Organocatalytic Imidazolium Ionic Liquids H/D Exchange Catalysts. The formation of imidazolium salt intimate (contact) ion pairs in solution Analysis of the Electronic Origin of the1JCHSpin−Spin Coupling Trend in 1-X-Cyclopropanes: Experimental and DFT Study Conformational behavior of cis-2-methoxy, cis-2-methylthio, and cis-2-methylselenocyclohexanol: a theoretical and experimental investigation Conformational preferences of 2-methoxy, 2-methylthio, and 2-methylselenocyclohexyl-N,N-dimethylcarbamate: a theoretical and experimental investigation Correspondence on "Preorganization and Cooperation for Highly Efficient and Reversible Capture of Low-Concentration CO2 by Ionic Liquids" Experimental and theoretical study of hyperconjugative interaction effects on NMR 1J(CH) scalar couplings Stereochemical dependence of 3JCH coupling constants in 2-substituted 4-t-butyl-cyclohexanone and their alcohol derivatives Gelatin and galactomannan-based scaffolds: Characterization and potential for tissue engineering applications. Dealing with supramolecular structure for ionic liquids: a DOSY NMR approach Regioselective preparation and NMR spectroscopy study of 2-chloro-4-ethoxy-quinoline for the synthesis of 2-((3-aminopropyl)amino)quinolin-4(1H)-one Difference between ²JC2H3 and ²JC3H2 spin-spin couplings in heterocyclic five- and six-membered rings as a probe for studying σ-ring currents: a quantum chemical analysis. Characterization of Gasoline by 1H Nuclear Magnetic Resonance and Chemometrics Stereochemical dependence of NMR geminal spin-spin coupling constants Canine metabolomics advances The effect of carbonyl group in the asymmetry of 3,4JCH coupling constants in norbornanones. NMR spin-spin couplings involving nuclei in the neighborhood of a carbonyl group.3JCH couplings in α-substituted acetamides
is author of	wds:Q52322829-C1509D2E-B93E-4C4E-8A2E-5D09EA4AF862 wds:Q85639683-CF47EC28-9FE5-46B4-AF08-E8146905056B wds:Q81467206-330A2D90-4C65-4CB6-B7DC-DF2D88A36507 wds:Q82910884-87208261-98E6-4068-848D-6EAE1BF601AF wds:Q82390813-6D6ADF51-9260-4CA0-8A89-68C42C4AC958 wds:Q79995164-9874B9C8-0426-4DAA-BB83-D3ABFA7953F2 wds:Q91107126-60C30CF3-E092-4014-9F2E-8E48FF9716EF wds:Q91907163-1F24F418-AF4F-40F2-AA19-5AB12A423301 wds:Q42793452-FAD42F90-4CFA-4080-A52C-FD282D83295A wds:Q31110173-7DED8059-E00D-48A9-9363-D138CA4CA526 wds:Q57782803-EF63CA55-8F5F-49DA-B3EF-738BE14813DA wds:Q51728724-3479DEAF-6CC3-45FE-9D88-F2F3262590A2 wds:Q58127411-C8885F4C-E252-4F96-8F81-36ECBD6A2548 wds:Q79808479-F1E61B9D-1872-49D0-AEEC-CED903F279ED wds:Q92751330-9A6B815A-6A04-44E3-945F-192E3EBDEC04 wds:Q46842111-F7281565-59AA-475E-AA49-6E584D2D5508 wds:Q46331134-A86CFC40-0515-41E7-80B1-2A8A6479CC2A wds:Q48289200-950E3946-3BF9-4821-9CA9-237960548EC1 wds:Q57782819-4ECE33AA-F0DF-4DD0-BFBF-0E88E757083D wds:Q90406618-D560654E-B8D2-44F9-ABCD-E4FCC410D9E0

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