About: Robert Vianello

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

researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) onderzoeker (nl)
rdfs:label	Robert Vianello (en) Robert Vianello (es) Robert Vianello (nl) Robert Vianello (sl) Robert Vianello (ast)
skos:prefLabel	Robert Vianello (en) Robert Vianello (es) Robert Vianello (nl) Robert Vianello (sl) Robert Vianello (ast)
name	Robert Vianello (en) Robert Vianello (es) Robert Vianello (nl) Robert Vianello (sl) Robert Vianello (ast)
Scopus author ID	wds:Q58085767-577DB115-2537-4CC7-8A26-D77C3FDC8983
Scopus author ID	6602140934
given name	wds:Q58085767-8DCFC29A-5179-4430-8DCD-D4766C693BD9
given name	Robert
instance of	wds:Q58085767-AEC0D840-C6F8-4170-BB60-A030A3898475
instance of	Homo sapiens
Loop ID	wds:Q58085767-8BF688AD-4A8C-4CCE-BEDF-EC41DFB1C8A4
Loop ID	107848
SICRIS researcher ID	wds:Q58085767-36323784-1BF6-4E0E-AF99-5E2794573325
SICRIS researcher ID	33294
occupation	wds:Q58085767-E27A66B5-F586-436B-A6AE-0F20A759870A
employer	wds:Q58085767-4266507A-6D23-4484-BCA3-B8E39719525A
CONOR.SI ID	wds:Q58085767-37C7FBD7-AF85-4E80-BE93-22BEE0EFFD43
sex or gender	wds:Q58085767-96b56aa3-422e-8a09-4af6-9a5e30fde0a2
VIAF ID	wds:Q58085767-52E96230-EF47-4DF2-84A5-27712D201280
family name	wds:Q58085767-2740C9DC-D3DB-436A-A83E-B583BBB91989
WorldCat Identities ID (superseded)	wds:Q58085767-ADCEE510-4227-4EA0-98B5-7C7A9F6D097D
VIAF ID	http://viaf.org/viaf/305741987
occupation	researcher
employer	Ruđer Bošković Institute
CONOR.SI ID	64691555
sex or gender	male
VIAF ID	305741987
family name	Vianello
WorldCat Identities ID (superseded)	viaf-305741987
ORCID iD	wds:Q58085767-8005D845-EB0B-4ECC-AE8E-C19CED3CAE4F
ORCID iD	https://orcid.org/0000-0003-1779-4524
ORCID iD	0000-0003-1779-4524
ResearcherID	wds:Q58085767-694E8DF7-DDB5-44B2-ABE8-9D0DD340DD09
Publons author ID	wds:Q58085767-31D0B1B0-F7EB-4BD8-986A-2C983CAF8A78
ResearcherID	J-3938-2012
Publons author ID	1328380
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58085767
is author of	Acidities of azoles in the gas phase and in DMSO: anab initioand DFT study Advances in determining the absolute proton affinities of neutral organic molecules in the gas phase and their interpretation: a theoretical account. How are Biogenic Amines Metabolized by Monoamine Oxidases? Fluorescent benzimidazo[1,2-a]quinolines: synthesis, spectroscopic and computational studies of protonation equilibria and metal ion sensitivity Novel pyrimidine-2,4-dione-1,2,3-triazole and furo[2,3-d]pyrimidine-2-one-1,2,3-triazole hybrids as potential anti-cancer agents: Synthesis, computational and X-ray analysis and biological evaluation. Computer aided design of organic superbases: the role of intramolecular hydrogen bonding The Quantum Nature of Drug-Receptor Interactions: Deuteration Changes Binding Affinities for Histamine Receptor Ligands Superbasicity of a bis-guanidino compound with a flexible linker: a theoretical and experimental study Design of Brønsted Neutral Organic Bases and Superbases by Computational DFT Methods: Cyclic and Polycyclic Quinones and [3]Carbonylradialenes In search of neutral organic superbases—iminopolyenes and their amino derivatives In search of ultrastrong Brønsted neutral organic superacids: a DFT study on some cyclopentadiene derivatives The origin of specificity and insight into recognition between an aminoacyl carrier protein and its partner ligase Examining Electrostatic Preorganization in Monoamine Oxidases A and B by Structural Comparison and pKa Calculations Irreversible Inhibition of Monoamine Oxidase B by the Antiparkinsonian Medicines Rasagiline and Selegiline: A Computational Study The engineering of powerful non-ionic superacids in silico—a DFT-B3LYP study of open chain polycyanopolyenes Rees polycyanated hydrocarbons and related compounds are extremely powerful Brønsted superacids in the gas-phase and DMSO—a density functional B3LYP study Interpretation of Brønsted Acidity by Triadic Paradigm: A G3 Study of Mineral Acids Physical origin of chemical phenomena: Interpretation of acidity, basicity, and hydride affinity by trichotomy paradigm Engineering Neutral Organic Bases and Superbases by Computational DFT Methods – Carbonyl Polyenes High acidity of polycyano azatriquinanes—theoretical prediction by the DFT calculations Strong Acidity of Some Polycyclic Aromatic Compounds Annulated to a Cyclopentadiene Moiety and Their Cyano Derivatives - A Density Functional B3LYP Study Towards highly powerful neutral organic superacids—a DFT study of some polycyano derivatives of planar hydrocarbons Design of Strong, Neutral Organic Superacids: DFT-B3LYP Calculations on Some Isobenzofulvene Derivatives Extending the acidity ladder of neutral organic superacids—a DFT-B3LYP study of deprotonation of nonacyanofluorene Tailoring of strong neutral organic superacids: DFT-B3LYP calculations on some fulvene derivatives The Acidity of Brønsted CH Acids in DMSO − The Extreme Acidity of Nonacyanocyclononatetraene Anionic versus Neutral Protonation—An Ab Initio Analysis with a Triadic Formula Quest for the Origin of Basicity: Initial vs Final State Effect in Neutral Nitrogen Bases Tuneable solid-state emitters based on benzimidazole derivatives: Aggregation induced red emission and mechanochromism of D-π-A fluorophores Transacylation in Ferrocenoyl-Purines. NMR and Computational Study of the Isomerization Mechanism Computational Study of the pKa Values of Potential Catalytic Residues in the Active Site of Monoamine Oxidase B. Quantum-chemical approach to determining the high potency of clorgyline as an irreversible acetylenic monoamine oxidase inhibitor. Empirical valence bond simulations of the hydride transfer step in the monoamine oxidase B catalyzed metabolism of dopamine. Exploring the biological promiscuity of high-throughput screening hits through DFT calculations What a Difference a Methyl Group Makes: The Selectivity of Monoamine Oxidase B Towards Histamine and N-Methylhistamine. On the Basicity of Conjugated Nitrogen Heterocycles in Different Media Engineering exceptionally strong oxygen superbases with 1,8-diazanaphthalene di-N-oxides Tandem β-elimination/hetero-michael addition rearrangement of an N-alkylated pyridinium oxime to an O-alkylated pyridine oxime ether: an experimental and computational study Binding of cadmium dication to glutathione facilitates cysteine SH deprotonation: A computational DFT study Polycyano Derivatives of some Organic Tri- and Hexacyclic Molecules Are Powerful Super- and Hyperacids in the Gas Phase and DMSO: Computational Study by DFT Approach Aromaticity of Rees-type hydrocarbons—a DFT computational study Basicity of Amines in the Gas Phase – Analysis of the Base-Strengthening Effect of anN-Trityl Group by Use of a Triadic Formula Comment on the Paper “On the Limits of Highest-Occupied Molecular Orbital Driven Reactions: The Frontier Effective-for-Reaction Molecular Orbital Concept”

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