about
How large is the conjugative stabilization of diynes?Investigation of a Putative Möbius Aromatic Hydrocarbon. The Effect of Benzannelation on Möbius [4n]Annulene AromaticityA stable, neutral diborene containing a B=B double bond.4n pi electrons but stable: N,N-dihydrodiazapentacenes.Diels-Alder Reaction of phosphaethene with 1,3-dienes: an ab initio study.A neutral Ga(6) octahedron: synthesis, structure, and aromaticity.Effects of fluorine on the structures and energetics of the propynyl and propargyl radicals and their anions.Nucleus-Independent Chemical Shifts (NICS) as an Aromaticity CriterionMyriad Planar Hexacoordinate Carbon Molecules Inviting SynthesisOn the Stability of Large [4n]AnnulenesThe existence of secondary orbital interactionsThe Concept of Protobranching and Its Many Paradigm Shifting Implications for Energy EvaluationsEvidence for d Orbital Aromaticity in Square Planar Coinage Metal ClustersHow do ring currents affect (1)h NMR chemical shifts?How aromatic are large (4n + 2)pi annulenes?A theoretical prediction of potentially observable lithium compounds with planar tetracoordinate carbonsPlanar tetracoordinate carbon atoms centered in bare four-membered rings of late transition metalsA trimetallic fulvalene-bridged dizirconocene-gallium complexPlanar, twisted, and trans-bent: conformational flexibility of neutral diborenesDownfield proton chemical shifts are not reliable aromaticity indicatorsA metallocene-complexed dibismuthene: Cp2Zr(BiR)2 (Cp = C5H5; R = C6H3-2,6-Mes2)Which NICS aromaticity index for planar pi rings is best?The geometry and electronic topology of higher-order charged Möbius annulenesThe Design of "Neutral" Carbanions with Intramolecular Charge Compensation
P50
Q28293860-7F9F0B37-6384-4CB3-80E0-EA1E78AB52FFQ29307590-C35ACA39-FA8F-4E66-9335-20B031A8FB7AQ34691782-993A5A6C-3817-4B38-B04B-2530CDDF6619Q42169572-322F5AF3-7BCD-4251-BD5D-D08BB8A0A755Q44256002-715705C6-BDBC-431D-B179-CAD06747F4AFQ46117808-C1AB7D91-5D25-4A08-BA8F-8AB6EEABED1AQ46764814-7269EF27-CAE3-456D-933E-E71A2DE119D2Q57229674-DE543015-449C-4EEC-84D3-1CB95B57F750Q58485349-4098CC75-3CB2-4911-8A01-BCBAB2DB19F0Q58485385-0BD2F7FB-E1D1-4C28-A1AD-0E678A005411Q60650780-3006A5DF-7B93-4CCA-861A-B1CB66AC6D21Q63973429-7B1174C1-49F0-48AC-A8DE-F903B379D601Q63973432-81ECE534-6FFF-4103-A639-492B6E954D50Q73046691-B1B2788B-D964-48F4-B236-FE6AE92E7C0BQ73116609-10473C67-2563-42E6-9EB2-671B30E7693BQ73868228-573B9F80-3F9F-4083-9F29-0FCB31F90DECQ79281716-0F7C6A7F-75A1-4B68-985A-95D02A6FC8C6Q79713149-7FD9B45D-44DE-4909-BDEF-174C38DEB781Q80742498-799434A0-BC52-4E3F-8EAB-B1D071FF2FBEQ81625935-147DBD28-E23A-4035-9081-D675697B4ADAQ81780440-43357457-84D4-4486-9C92-A9AB4A03F41CQ82631648-BB7B57DB-1EA7-4DCE-B375-07FF9082DA5DQ84305602-056B9452-ED53-4767-AAB6-3465A0760E1BQ87110994-C55076C5-60C0-4199-9354-558D957B2794
P50
description
researcher
@en
name
Chaitanya S Wannere
@en
Chaitanya S Wannere
@nl
type
label
Chaitanya S Wannere
@en
Chaitanya S Wannere
@nl
prefLabel
Chaitanya S Wannere
@en
Chaitanya S Wannere
@nl
P106
P31
P496
0000-0002-9569-7642