Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
about
Comparison of Oxidative Aromatic Coupling and the Scholl ReactionVertically π-expanded imidazo[1,2-a]pyridine: the missing link of the puzzle.New advances in nanographene chemistry.Concise synthesis of 3D π-extended polyphenylene cylinders.Phosphorus-Containing Polycyclic Aromatic Hydrocarbons.π-extended [12]cycloparaphenylenes: from a hexaphenylbenzene cyclohexamer to its unexpected C2-symmetric congener.Tethered 2 + 2 + 2 cycloaddition reactions of cobalt-cycloheptyne complexes.A divergent route to core- and peripherally functionalized diazacoronenes that act as colorimetric and fluorescence proton sensors.Rhodium and palladium complexes of a pyridyl-centred polyphenylene derivative.Exploration of pyrazine-embedded antiaromatic polycyclic hydrocarbons generated by solution and on-surface azomethine ylide homocoupling.Cationic Nitrogen-Doped Helical Nanographenes.Carbon-rich "Click" 1,2,3-triazoles: hexaphenylbenzene and hexa-peri-hexabenzocoronene-based ligands for Suzuki-Miyaura catalysts.Methoxy functionalisation: exerting synthetic control of the supramolecular and electronic structure of nitrogen-doped nanographenes.Intriguing Diels-Alder products: chiral centres with an added twist.Structure-property relationships and (1)O)2) photosensitisation in sterically encumbered diimine Pt(II) acetylide complexes.Photochemical and oxidative cyclisation of tetraphenylpyrroles.Fused π-Extended Truxenes via a Threefold Borylation as the Key Step.Synthesis of a peripherally conjugated 5-6-7 nanographene.Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance.Block Copolymer Templating as a Path to Porous Nanostructured Carbons with Highly Accessible Nitrogens for Enhanced (Electro)chemical PerformanceFrom Nanographene and Graphene Nanoribbons to Graphene Sheets: Chemical SynthesisKationische stickstoffdotierte helikale Nanographene
P2860
Q29395008-FCCD01A4-48C2-4856-8C42-76898C15823FQ33358501-7B9EED3D-0BBD-46D8-8D80-5CC34E8D38A9Q38549476-60E2E7C1-2EE7-494A-831A-FE27D1EA4134Q39266589-001DD52C-CAA5-4A7F-A3A2-0EC410540229Q39369765-1065DDF3-A3CF-47EA-98C6-B26497688FA3Q41011948-B71B9943-320A-4DBF-8763-E604B95C21C0Q44696710-86D604AA-BF33-4850-B3FF-7FBA0A6151EDQ46093311-9294B073-F57C-455C-8D10-52797CE650C8Q46837985-FE2C2E3E-9108-4244-8274-BFC5549197F2Q47096832-42761022-65B3-444C-A9CD-2B79826889D5Q48054035-A7D068AD-FA43-4837-AA6C-792F17F1A38FQ48272466-F3067F32-FE6C-40BA-97DF-073ECA0C62B9Q50452067-052F4B6B-6DB5-419A-8568-E94D1FEDFC58Q50463853-C8398A25-BE8E-4B76-B61A-7172A1CEA783Q50471289-D87EEA3A-8F26-4D81-B510-16808FD167A8Q52836213-6A046CB7-CDAC-453A-ABBD-7D2747749B85Q53190863-C1FE125B-355D-498A-8B79-D78E39E08F8EQ55213987-9ACA3931-9679-4F57-9EDB-B1123EED08F6Q55413760-E21AD53F-C1FD-4A42-A2E5-199D40566D3CQ56904655-257F8D2B-A5CF-4AB1-8283-048EA923DED4Q57946781-9541673F-2999-46C9-842C-85C625358E0AQ59315217-72E36AEC-F2DC-4A69-9DA5-B0A0A06DA27B
P2860
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
description
2002 nî lūn-bûn
@nan
2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
@ast
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
@en
type
label
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
@ast
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
@en
prefLabel
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
@ast
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules.
@en
P356
P1476
Heterosuperbenzenes: a new family of nitrogen-functionalized, graphitic molecules
@en
P2093
Daniel J Gregg
Rethi Madathil
P304
P356
10.1021/JA017394U
P407
P577
2002-04-01T00:00:00Z