about
Probing the Origin of Challenge of Realizing Metallaphosphabenzenes: Unfavorable 1,2-Migration in Metallapyridines Becomes Feasible in Metallaphosphabenzenes.Recent developments and future prospects of all-metal aromatic compounds.Usefulness of the σ-Aromaticity and σ-Antiaromaticity Concepts for Clusters and Solid-State Compounds.Synthesis of tetra- and octa-aurated heteroaryl complexes towards probing aromatic indoliumsRecent Advances in Metallaaromatic Chemistry.Synthesis and Characterization of a Metallacyclic Framework with Three Fused Five-membered Rings.Metallapentalenofurans and Lactone-Fused Metallapentalynes.Understanding the molecular switching properties of octaphyrins.Synthesis of aromatic ruthenabenzothiophenes via C-H activation of thiophenes.Triplet State Aromaticity: NICS Criterion, Hyperconjugation, and Charge Effects.Revealing the thermodynamic driving force for ligand-based reductions in quinoids; conceptual rules for designing redox active and non-innocent ligands.Multiyne chains chelating osmium via three metal-carbon σ bonds.Rational Design and Synthesis of Unsaturated Se-Containing Osmacycles with σ-Aromaticity.Influence of the Transition-Metal Fragment on the Reactivity of Metallaanthracenes.Iron-Catalyzed Olefin Metathesis with Low-Valent Iron Alkylidenes.Peculiar All-Metal σ-Aromaticity of the [Au2 Sb16 ](4-) Anion in the Solid State.Syntheses of Amino-Substituted Iridabenzofurans and Subsequent Selective N-Functionalisation.The aromaticity of dicupra[10]annulenes.Synthesis and Characterization of Dirhenadehydro[12]annulenes.σ Aromaticity Dominates in the Unsaturated Three-Membered Ring of Cyclopropametallapentalenes from Groups 7-9: A DFT Study.Boosting catalyst activity in cis-selective semi-reduction of internal alkynes by tailoring the assembly of all-metal aromatic tri-palladium complexes.A Cyclotriborane Dianion and the Triboron Cation: "Light Ends" of the Hückel Rule.Constraint of a ruthenium-carbon triple bond to a five-membered ring.The effect of the metal fragment on the aromaticity and synchronicity of the gold(i)-catalysed divinylcyclopropane–cycloheptadiene rearrangement
P2860
Q37035296-0033922C-A869-4FEF-B57C-472F2645429CQ38997550-11AC44FA-7BC9-4FF5-9DD1-43E70FE889A5Q39359039-B83FA556-BA52-4C9B-BD8C-519C193C71F9Q41981150-2E4B9D6B-1387-41D0-A5B4-FB7518759F93Q46250419-58BAB194-5186-48D9-934F-29B3BA31F106Q46355459-1BDAC6F3-F6B7-4442-BF38-327A82E59C43Q46403889-CEF55362-C7E9-4998-8864-1671ABF9A6ACQ46588447-1731692B-1743-427C-8CD0-8718ADA82407Q46623759-71439FEF-43FC-4BFE-9283-37E465A26A5CQ46648135-7FBEC491-8D45-4B3B-8D38-3B1F69238DE4Q47103426-9EDD8B56-4855-40B7-B63E-21610FBD7076Q47142741-F76B3E99-5EC0-41B9-B5DA-0EA2456D6D24Q47575891-F5B39A12-F108-42BC-812E-8A86AA80B6A8Q48043958-269E98A1-5D47-453A-8BFF-14063E6A1A37Q48059623-DE41B747-D53B-433D-BDB5-13AA75C20AC8Q48215060-5148C574-E69C-4980-81D7-760EC0F5BDCBQ48346141-FD838D62-5F15-4BAA-B99A-89E9735463B6Q48353942-7D66CB17-0FEE-44C7-B3FB-9662E538794EQ51352929-6CA1B27B-28D6-41E8-9F29-FFF4C2D55916Q51648960-A20ABDEF-E8BF-4203-BA3A-C5B6BA61E5EEQ53591871-B62E5192-B68E-4959-8D88-AAF7E6381A87Q53641874-61BA4264-891F-4A08-853C-675D4E3A1A49Q55423346-3AF009B7-A72E-4801-A97B-87AE7C9E4E47Q58447169-F79CC054-1A88-4287-B5B1-439E75F2485D
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Aromaticity of metallabenzenes and related compounds.
@en
type
label
Aromaticity of metallabenzenes and related compounds.
@en
prefLabel
Aromaticity of metallabenzenes and related compounds.
@en
P2860
P356
P1476
Aromaticity of metallabenzenes and related compounds.
@en
P2093
Gabriel Merino
Gernot Frenking
P2860
P304
P356
10.1039/C5CS00004A
P577
2015-02-18T00:00:00Z