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Reversible Bergman cyclization by atomic manipulationBond-order discrimination by atomic force microscopy.Tunable Band Alignment with Unperturbed Carrier Mobility of On-Surface Synthesized Organic Semiconducting WiresSubstrate-Independent Growth of Atomically Precise Chiral Graphene NanoribbonsCopper-catalyzed asymmetric conjugate addition of Grignard reagents to cyclic enones.Characterizing aliphatic moieties in hydrocarbons with atomic force microscopy.Cycloaddition of benzyne to SWCNT: towards CNT-based paddle wheels.Domino Diels-Alder cycloadditions of arynes: new approach to elusive perylene derivatives.Aryne-mediated syntheses of structurally related acene derivatives.One-pot synthesis of sterically congested large aromatic hydrocarbons via 1,4-diphenyl-2,3-triphenylyne.Highly enantioselective Cu-catalysed asymmetric 1,4-addition of diphenylzinc to cyclohexenone.Diastereoselective remote C-H activation by hydroboration.Stereoselective tandem cascade furan cycloadditions.Generation and Characterization of a meta-Aryne on Cu and NaCl Surfaces.On-Surface Route for Producing Planar Nanographenes with Azulene Moieties.Unraveling the Electronic Structure of Narrow Atomically Precise Chiral Graphene Nanoribbons.On-surface generation and imaging of arynes by atomic force microscopy.Microwave-induced covalent functionalization of few-layer graphene with arynes under solvent-free conditions.Decacene: On-Surface Generation.Survival of spin state in magnetic porphyrins contacted by graphene nanoribbons.Site-selective reversible Diels-Alder reaction between a biphenylene-based polyarene and a semiconductor surface.Doping of Graphene Nanoribbons via Functional Group Edge Modification.Tetracene Formation by On-Surface Reduction.Imaging the electronic structure of on-surface generated hexacene.Unraveling the Molecular Structures of Asphaltenes by Atomic Force Microscopy.Bottom-up synthesis of multifunctional nanoporous graphene.Atomic Force Microscopy for Molecular Structure Elucidation.1,7-Naphthodiyne: a new platform for the synthesis of novel, sterically congested PAHs.Studying an antiaromatic polycyclic hydrocarbon adsorbed on different surfaces.A C60-aryne building block: synthesis of a hybrid all-carbon nanostructure[19]Dendriphene: a 19-Ring Dendritic NanographeneElectronic Resonances and Gap Stabilization of Higher Acenes on a Gold SurfaceOn-surface synthesis of superlattice arrays of ultra-long graphene nanoribbonsStraightforward Synthesis of a Vicinal Double-Bridgehead Iodo Trimethylsilyl Octacycle: Unprecedented Lack of Reactivity of the Silyl Group in the Presence of Fluoride AnionsHeavy Oil Based Mixtures of Different Origins and Treatments Studied by Atomic Force MicroscopyFrom Perylene to a 22-Ring Aromatic Hydrocarbon in One-PotAtomic Force Microscopy Identifying Fuel Pyrolysis Products and Directing the Synthesis of Analytical StandardsOn the Mechanism of the Copper-Catalyzed Enantioselective 1,4-Addition of Grignard Reagents to α,β-Unsaturated Carbonyl CompoundsRevisiting Kekulene: Synthesis and Single-Molecule ImagingMono- versus bidentate ligands in rhodium-catalyzed asymmetric hydrogenation. A comparative rate study
P50
Q29302518-29426412-5BA8-4291-BAB3-A1CF3994C72EQ34300097-341DE6D0-82AB-4DAA-A956-9AFA29E0986CQ36664439-03DFFFB2-72B7-40EA-B01D-12E9396B3115Q37298996-F28A8788-AEDB-4A35-853E-59421E2C9BC8Q37649342-61E51FDB-AC60-4FC6-8CF7-CDA99FDD9DC4Q41848484-6D539551-042E-47F5-B876-8EA235C66BD5Q42929744-7CE96FBE-4BD5-43F8-9576-1D327C90AC0BQ42969778-37DB4235-D0B5-4F26-A920-7E0E5F96AEC1Q43008269-81D8C016-2F64-4A1A-BB96-F73BB8EFB57DQ44370879-8BFD483E-FD1A-40E7-917E-07027F1CD69BQ45015370-93292B01-7291-4378-8A71-0CDFD6F55EC4Q45047775-8811BDD6-0579-46FE-ACC9-4884F5B09561Q45752286-2DBDCABE-6171-468A-87D5-78EB662B6911Q48051768-C7F1096B-9499-496A-A1DB-615DF87BDC56Q48131944-94D197B8-175A-405C-AC9A-FC27BFD7B06DQ48152504-6FB78C60-61B3-40AF-824B-DCFF374126D3Q48155610-B7CD7561-87EE-4792-A003-5FD1946A6B1CQ48244433-852750F2-1E91-4CCD-BEE6-697F5F8CFBB1Q48296638-EC160AF3-3097-4CBB-8059-D4A74FC39BBBQ49724041-6E4A1C51-5BD1-48CC-B71E-2D1D0A244A46Q52592185-B4151663-3202-4402-8F89-712DD84ACBE9Q52764969-A7F2693C-A9F6-4A5E-93A6-31CB2EB53996Q52881284-3615BF99-0DFB-4A68-845F-A79272031D40Q53541742-DD0371E5-53CF-466D-A5BE-4F9E23924007Q53622613-F3F68795-A104-49C0-BE58-8C0B59B1ED44Q53823172-13D21987-2022-4D05-881E-8C9736B72834Q53840929-36A3053F-9332-4D3E-816E-198D5B625B4BQ54768961-86DFC6EB-4C5F-4291-AC1F-3584A0EAD6FEQ55175973-CD250BDE-B689-4434-9137-1540A211529DQ57156715-934455D8-A352-4172-AB9E-AE66485C1E7BQ57456520-A5EDCA6C-3BC2-4EAC-90FE-43F60DB2DC3BQ57920618-9B19B703-2DB5-4E13-9AA2-C5ACC40570E6Q58203179-5870CE2A-1FEC-409B-9A87-6E1D8B358835Q58856685-C047D836-8798-4CDC-8C53-279785F5621BQ63350297-E0252855-E378-4351-B4D4-9BF7E79D2B19Q63350310-78D15F08-589E-4F49-A6B8-C7BDE29C585CQ63350512-A9C90836-15B3-4524-8094-DFD3FFAD4F38Q63982205-F5AE42BE-74E1-423E-A2C3-0EB17D5C8AF2Q71467895-41CB1CD3-44F4-41F2-9BF6-5A10B9030730Q72990875-F0C8B136-5C8A-424F-A34B-460F7488E7BB
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Diego Peña
@ast
Diego Peña
@en
Diego Peña
@es
Diego Peña
@nl
Diego Peña
@sl
type
label
Diego Peña
@ast
Diego Peña
@en
Diego Peña
@es
Diego Peña
@nl
Diego Peña
@sl
prefLabel
Diego Peña
@ast
Diego Peña
@en
Diego Peña
@es
Diego Peña
@nl
Diego Peña
@sl
P106
P21
P31
P496
0000-0003-3814-589X