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On the mechanism of the thermal retrocycloaddition of pyrrolidinofullerenes (retro-Prato reaction)Retro-cycloaddition reaction of pyrrolidinofullerenesTuning the electronic properties of nonplanar exTTF-based push-pull chromophores by aryl substitution.Buckyballs.Synthesis and radical coupling of pyridine-bridged pi-extended tetrathiafulvalene (TTF)-type donors and push-pull analogues.Large exTTF-based dendrimers. Self-assembly and peripheral cooperative multiencapsulation of C60.Metal nitride cluster fullerene M3N@C80 (M=Y, Sc) based dyads: synthesis, and electrochemical, theoretical and photophysical studies.Microsecond charge separation upon photoexcitation of gold nanoparticles in imidazolium ionic liquids.Fullerene dimers (C60/C70) for energy harvesting.Electron donor-acceptor interactions in regioselectively synthesized exTTF(2)-C(70)(CF(3))(10) dyads.Macrocyclic hosts for fullerenes: extreme changes in binding abilities with small structural variations.Unambiguous one-molecule conductance measurements under ambient conditions.Stability of single- and few-molecule junctions of conjugated diamines.A detailed experimental and theoretical study into the properties of C60 dumbbell junctions.Controlling the spatial arrangement of organic magnetic anions adsorbed on epitaxial graphene on Ru(0001).Electron transfer in Me-blocked heterodimeric alpha,gamma-peptide nanotubular donor-acceptor hybridsHydrogen-bonding motifs in fullerene chemistry.Curves ahead: molecular receptors for fullerenes based on concave-convex complementarity.Fullerene for organic electronics.Organic photovoltaics: a chemical approach.Pyrazolinofullerenes: a less known type of highly versatile fullerene derivatives.Molecular self-assembly at solid surfaces.The chemistry of pristine graphene.Enantioselective cycloaddition of münchnones onto [60]fullerene: organocatalysis versus metal catalysis.Incorporating single molecules into electrical circuits. The role of the chemical anchoring group.Morphological characterization of fullerene-androsterone conjugates.Thermodynamically stable [4 + 2] cycloadducts of lanthanum-encapsulated endohedral metallofullerenes.Fingerprints of Through-Bond and Through-Space Exciton and Charge π-Electron Delocalization in Linearly Extended [2.2]Paracyclophanes.Small molecule BHJ solar cells based on DPP(TBFu)2 and diphenylmethanofullerenes (DPM): linking morphology, transport, recombination and crystallinity.Glycofullerenes inhibit viral infection.Chemical functionalization and characterization of graphene-based materials.Charge-transfer-induced structural rearrangements at both sides of organic/metal interfaces.Formation of self-assembled chains of tetrathiafulvalene on a Cu(100) surface.Multivalent Glycosylated Nanostructures To Inhibit Ebola Virus Infection.Charge transfer-assisted self-limited decyanation reaction of TCNQ-type electron acceptors on Cu(100).New challenges in fullerene chemistry.Stereodivergent synthesis of chiral fullerenes by [3 + 2] cycloadditions to C₆₀.New concepts and applications in the macromolecular chemistry of fullerenes.Donor-acceptor conjugates of lanthanum endohedral metallofullerene and pi-extended tetrathiafulvalene.Fullerene sugar balls.
P50
Q28277836-7713940E-D88A-4EBC-BA8E-D560867EE5C6Q28278358-DADE1573-E70F-4E0F-8243-7CF7F73AA306Q30576372-E987A43E-BA0A-4B75-8A8E-B59555EDA4D7Q30608629-BDCC818F-E62B-4A09-946B-8F49D17B382EQ31108039-870205F4-330C-4D5F-B105-EE2760CC6D74Q33352231-DB227031-ABA3-4DF0-9FC3-4245295DC30DQ33389232-260A2DA2-0B45-4860-8D90-47281ACF8093Q33392902-3F1D3AA2-D0E3-4A75-B73F-FC598EC51321Q33515307-B161ACE2-3322-4236-93BE-2DD8AA9536FFQ33538111-8B1ED4A8-19F6-474E-87D4-BFFA1D02E69EQ33820098-6A7C1D95-E2F5-4552-8F77-3BE2AD912D3DQ33891332-F212D649-D73C-4DCF-A84E-98421705FBE1Q34615242-EC0182EA-6FE2-49A8-8612-758ACC04CEA2Q34695196-FB55575E-4B45-42B5-862D-CEBCA0294596Q35405918-FD58536C-9650-4A72-A7B4-44F9F733CDB4Q35720373-EB104CB6-167E-46E3-9F72-95D08CDCA34FQ36183880-8C1DD9AB-EF7E-4A7B-8809-E518AD3A185EQ37224383-85B807AA-73CA-4A7F-9FBB-C9B2A74464D9Q37545417-E6C8675A-9138-4687-8CF0-FB46177C3A77Q37760441-90A393A6-075A-4732-BB6B-DC167BFCCB83Q37890266-FD6DDBE6-6DCC-4977-BB31-4CD7F87C3F2DQ37932461-83B53C88-8733-489A-90FC-EF0901639184Q38094127-1824D8CA-887C-458A-9973-8CE271FCBD10Q38276457-02C33140-8E76-40A5-9491-8A522E138A31Q38293135-BAA52FBD-E966-443B-8520-FB7B44FFA1FFQ38969214-C91FD644-AC71-42E9-B495-32C293EC48B2Q38969446-FE009A48-08DF-47B9-928B-08DFA2D55FA3Q38974206-CA94A25B-0A82-49FF-9CB3-ADDFA146099EQ39206154-FD62DC21-4F4A-4AF9-ABF6-CE959890B920Q39217742-8D218E4E-0116-4DCB-9200-E54D9EED3108Q39431944-47DF37E2-25AB-4D50-8E60-3A7D78DA24A7Q39929943-F217FAB7-BB16-426B-B79C-1D5447A2C035Q40000732-FD699E17-28F8-49B6-A566-FB2CFF222D15Q40061795-BE1CCBAF-D366-46BB-A1A6-16D0171C900FQ40154400-04EC14F0-B823-4063-A35B-AF8673A824FDQ40325028-4251AE3A-CB8B-4740-9F2F-23A955DDA34EQ41915757-3A84CF38-9044-45BF-B131-32FC01E5A9E9Q42924308-C2DB5997-71EC-487F-BD99-7447CE7191AAQ43057381-9BE6E6D7-0992-487B-A8DA-B6651CEDE677Q43087919-797745FC-ED77-4371-921A-A202F8EF8CE7
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Nazario Martín
@ast
Nazario Martín
@en
Nazario Martín
@es
Nazario Martín
@nl
Nazario Martín
@sl
type
label
Nazario Martín
@ast
Nazario Martín
@en
Nazario Martín
@es
Nazario Martín
@nl
Nazario Martín
@sl
prefLabel
Nazario Martín
@ast
Nazario Martín
@en
Nazario Martín
@es
Nazario Martín
@nl
Nazario Martín
@sl
P1053
B-4329-2008
P106
P1153
7401810319
P21
P31
P3829
P496
0000-0002-5355-1477
P569
2000-01-01T00:00:00Z