about
Removal of the emerging contaminant bisphenol A by an ureasil-PEO hybrid membrane: experimental study and molecular dynamic simulation.Polyacetylenes from the leaves of Vernonia scorpioides (Asteraceae) and their antiproliferative and antiherpetic activities.A computational study of [2.2]cyclophanes.Evaluation of Electron Donation as a Mechanism for the Stabilisation of Chalcogenate-Protected Gold Nanoclusters.Sesquiterpene lactones from Vernonia scorpioides and their in vitro cytotoxicity.Synthesis and Solvatochromism of Substituted 4-(Nitrostyryl)phenolate Dyes.Ureasil-poly(ethylene oxide) hybrid matrix for selective adsorption and separation of dyes from water.How the electron-deficient cavity of heterocalixarenes recognizes anions: insights from computation.In vivo and in silico anti-inflammatory mechanism of action of the semisynthetic (-)-cubebin derivatives (-)-hinokinin and (-)-O-benzylcubebin.Tuning Heterocalixarenes to Improve Their Anion Recognition: A Computational Approach.The two faces of hydrogen-bond strength on triple AAA-DDD arrays.Quest for Insight into Ultrashort C–H···π Proximities in Molecular “Iron Maidens”Ruthenium(II)/4,6-dimethyl-2-mercaptopyrimidine complexes: Synthesis, characterization, X-ray structures and in vitro cytotoxicity activities on cancer cell linesAromaticity and Homoaromaticity in Methano[10]annulenesA computational study of tetrafluoro-[2.2]cyclophanesThe nature of the interactions between Pt4 cluster and the adsorbates *H, *OH, and H2OComputational study about through-bond and through-space interactions in [2.2]cyclophanesThe nature of Ru-NO bonds in ruthenium tetraazamacrocycle nitrosyl complexes--a computational studyNitro-substituted 4-[(phenylmethylene)imino]phenolates: solvatochromism and their use as solvatochromic switches and as probes for the investigation of preferential solvation in solvent mixturesNanoparticle translocation through a lipid bilayer tuned by surface chemistryProton-induced generation of remote N-heterocyclic carbene-Ru complexesCyclic trinuclear copper(I), silver(I), and gold(I) complexes: a theoretical insightNo need for a re-examination of the electrostatic notation of the hydrogen bonding: a commentRuthenium(II) complexes of N-heterocyclic carbenes derived from imidazolium-linked cyclophanesRu-NO and Ru-NO2 bonding linkage isomerism in cis-[Ru(NO)(NO)(bpy)2](2+/+) complexes - a theoretical insightCopaifera duckei Oleoresin and Its Main Nonvolatile Terpenes: In Vitro Schistosomicidal PropertiesPolar Order and Symmetry Breaking at the Boundary between Bent-Core and Rodlike Molecular Forms: When 4-Cyanoresorcinol Meets the Carbosilane End GroupCoordination among Bond Formation/Cleavage in a Bifunctional-Catalyzed Fast Amide Hydrolysis: Evidence for an Optimized Intramolecular N-Protonation EventShedding Light on the Hydrolysis Mechanism of cis, trans-[Ru(dmso)4Cl2] Complexes and Their Interactions with DNA-A Computational PerspectiveUnderstanding the interplay between π-π and cation-π interactions in [janusene-Ag]+ host-guest systems: a computational approachSynthesis, characterization and biological evaluation of new manganese metal carbonyl compounds that contain sulfur and selenium ligands as a promising new class of CORMsESI-QTof-MS characterization of hirsutinolide and glaucolide sesquiterpene lactones: Fragmentation mechanisms and differentiation based on Na+ /H+ adducts interactions in complex mixture
P50
Q38712698-BA405765-7CAF-415F-8FB8-C67F6942A586Q39111422-B15362F0-B210-4E07-B85F-697644B337A2Q39368389-E9523D1A-8D98-4A8B-9989-BAF3A0FFE3E3Q39626844-CEE4FD9D-DEA2-4ADF-9F3A-468C567DCFB6Q39685435-51168F20-023F-420A-8ECA-7AF04A17B200Q40699806-0DEE99AF-5431-4809-A13A-865C440CD7D3Q50224581-329ECED9-82A9-45E0-9DDA-3EDD6A01848CQ50238449-02A75702-4FAF-4405-BE16-13B5E142BEBDQ51272280-EB3D99A9-DC1C-43BA-A555-D06FCC83BCE9Q52354724-E2E0DB1A-4A33-4843-BC24-6BC4AF4C922BQ54518970-C5F3B1A4-CFE4-4654-92FF-B3E76B35C7DBQ57587709-EDA80D12-53CD-424C-A49F-3D9B1E331DF8Q58860580-459D7DD1-D2FE-456A-8B16-C1E0150135F5Q79458932-FAC081DD-41DF-44D1-A231-41B676585962Q79680403-B75A983C-FB32-4DC5-9996-C79949D6A0A2Q79680416-756BFC19-BF0D-4B03-B604-A2C43C1AF80CQ79762596-C1C68EA7-22CA-40F4-BDE7-FDC7DB53B6DBQ84118134-6C006616-4DB9-4CA5-8927-FD3D2EB47295Q85248685-2B7A7218-9FD6-461E-9E38-5EAD4CB450F4Q85637962-145DCC07-CCD9-49D4-9D3B-D6D76891DEE2Q85933250-B23721CE-2A1B-4DBB-916D-6C868D6501CDQ85938525-000232CD-99EE-42F6-8908-EB6CA40AC3A4Q86658084-796A5061-5030-4879-BBA4-78F924A22951Q87631705-0FCE8D3D-8739-4E9F-B6B4-A44C38B83186Q87781339-E14A8505-E7D2-4DED-9248-0EF005F4532DQ87983728-67DD3C46-D3AE-4DEE-A02F-E77F1E9EB35BQ89365345-660ABD42-ED59-4B07-9EFE-D63D900E6D56Q90186109-2168E247-F032-40D8-AE7B-641ADFE87959Q90697490-F59BF703-C497-40F7-93AF-E9AEE0BEA4F2Q92686095-6D4818FF-8B93-431A-B231-C86E604B9274Q92806271-25F70007-9472-4E3D-9490-863D8CEBA552Q93055449-4DCB0732-E89E-47A8-AC78-05B994763C77
P50
description
researcher ORCID ID = 0000-0002-6455-7831
@en
wetenschapper
@nl
name
Giovanni F. Caramori
@ast
Giovanni F. Caramori
@en
Giovanni F. Caramori
@es
Giovanni F. Caramori
@nl
type
label
Giovanni F. Caramori
@ast
Giovanni F. Caramori
@en
Giovanni F. Caramori
@es
Giovanni F. Caramori
@nl
prefLabel
Giovanni F. Caramori
@ast
Giovanni F. Caramori
@en
Giovanni F. Caramori
@es
Giovanni F. Caramori
@nl
P106
P1153
9846482000
P21
P31
P496
0000-0002-6455-7831