sameAs
New family of aminophenalenyl-based neutral radical molecular conductors: synthesis, structure, and solid state properties.Resonating valence bond ground state in oxygen-functionalized phenalenyl-based neutral radical molecular conductors.The non-innocent phenalenyl unit: an electronic nest to modulate the catalytic activity in hydroamination reaction.Development of a facile antibody-drug conjugate platform for increased stability and homogeneityInterface-engineered templates for molecular spin memory devices.Singlet oxygen mediated DNA degradation by copper nanoparticles: potential towards cytotoxic effect on cancer cells.Assembling heterometals through oxygen: an efficient way to design homogeneous catalysts.Synthesis, structure, spectroscopic characterization, and protein binding affinity of new water-soluble hetero- and homometallic tetranuclear [Cu(II)2Zn(II)2] and [Cu(II)4] clusters.Substitution effect on phenalenyl backbone in the rate of organozinc catalyzed ROP of cyclic esters.Abnormal N-heterocyclic carbene main group organometallic chemistry: a debut to the homogeneous catalysis.A new face of phenalenyl-based radicals in the transition metal-free C-H arylation of heteroarenes at room temperature: trapping the radical initiator via C-C σ-bond formation.Exploring Closed-Shell Cationic Phenalenyl: From Catalysis to Spin Electronics.Highly Active Carbene Potassium Complexes for the Ring-Opening Polymerization of ε-Caprolactone.Polyethyleneimine functionalized single-walled carbon nanotubes as a substrate for neuronal growth.Accessing Heterobiaryls through A Transition Metal-Free C-H Functionalization.Open-Shell Phenalenyl in Transition Metal-Free Catalytic C-H Functionalization.Metal-Free Reduction of CO2 to Methoxyborane under Ambient Conditions through Borondiformate Formation.Tuning the redox non-innocence of a phenalenyl ligand toward efficient nickel-assisted catalytic hydrosilylation.ChemInform Abstract: Phenalenyl-Based Ligand for Transition Metal Chemistry: Application in Henry ReactionChemInform Abstract: Assembling Zirconium and Calcium Moieties Through an Oxygen Center for an Intramolecular Hydroamination Reaction: A Single System for Double ActivationAssembling Zirconium and Calcium Moieties through an Oxygen Center for an Intramolecular Hydroamination Reaction: A Single System for Double ActivationAssembling Zirconium and Calcium Moieties through an Oxygen Center for an Intramolecular Hydroamination Reaction: A Single System for Double ActivationPhenalenyl-Based Molecules: Tuning the Lowest Unoccupied Molecular Orbital to Design a CatalystOxygen-Bridged Hybrid Metallocene−Nonmetallocene Polymetallic Catalysts of Group 4 Metals for Bimodal Activity in Olefin Polymerization: Synthesis, Characterization, and Theoretical Investigation†Chiral “P–N–P” ligands, (C20H12O2)PN(R)PY2 [R=CHMe2, Y=C6H5, OC6H5, OC6H4-4-Me, OC6H4-4-OMe or OC6H4-4-tBu] and their allyl palladium complexesFenton-Reaction-Accelerable Magnetic Nanoparticles for Ferroptosis Therapy of Orthotopic Brain TumorsGraphene oxide-phenalenyl composite: transition metal-free recyclable and catalytic C-H functionalizationSoluble graphene derived from graphite fluorideThe First Electronically Stabilized Phenalenyl Radical: Effect of Substituents on Solution Chemistry and Solid-State StructurePhenalenyl in a Different Role: Catalytic Activation through the Nonbonding Molecular OrbitalConstruction of oxygen-bridged multimetallic assembly: dual catalysts for hydroamination reactionsSoluble molecular compounds with the Mg-O-Al structural motif: a model approach for the fixation of organometallics on a MgO surfaceSynthesis, structural characterization, catalytic properties, and theoretical study of compounds containing an Al-O-M (M = Ti, Hf) coreSynthesis, structural characterization, and theoretical investigation of compounds containing an Al-O-M-O-Al (M=Ti, Zr) coreAbnormal N-heterocyclic carbene palladium complex: living catalyst for activation of aryl chlorides in Suzuki-Miyaura cross couplingPhenalenyl-based organozinc catalysts for intramolecular hydroamination reactions: a combined catalytic, kinetic, and mechanistic investigation of the catalytic cycleInterstellar molecules: guides for new chemistryGroup 14 hydrides with low valent elements for activation of small moleculesIntroduction of abnormal N-heterocyclic carbene as an efficient organocatalyst: ring opening polymerization of cyclic estersChemoselective reduction of the carbonyl functionality through hydrosilylation: integrating click catalysis with hydrosilylation in one pot
P50
Q30991036-D3EEC4C8-0200-4D1D-ABA7-D8D89A192FCEQ31031954-99CF3AE3-64C3-4D91-AC77-7A60B5BEE351Q41829065-8A8BCEC6-5ED0-4D7A-A725-E127568F8354Q42293596-A05EEC21-FFC5-4ED6-A693-6B7282367FA2Q42683971-467803D5-C7D8-456B-BA5F-E4BD4A5AD142Q42712250-50811EC0-C082-41A4-80C7-45BFAC3669E3Q43264637-34A113F3-C25C-4B4C-832F-738F51523556Q44449892-5A1FB706-0EAF-4C47-A606-D037DC86B07BQ44530410-BF1233AB-81D5-4E71-B8B2-8E9B78D95888Q44885528-62A0B2DC-1F4E-4A06-B73C-9EC84FD0AB97Q46256471-DE461A29-3B8E-4FB6-BC7A-048958160A9EQ47970539-ED06E138-26E0-4ADA-B65F-62B39CB6CC72Q48048806-20D99802-19AA-498A-9ECF-2EE72D4F0163Q48468120-1451551E-F975-49AD-9961-B4145909E6DCQ50047022-0A5241B5-D9B9-4893-8056-2CE67C2A2E54Q50672861-4A1147F3-98FC-4B25-ACB2-6BF7FDA2F990Q53551494-54ADC70F-243E-40E8-8525-0614657E08E2Q55004313-CABF050E-0303-47BD-865F-D7CCBE9FA6B1Q57905776-E5C4DDB8-0069-4BE8-8BBC-9F0A36C2882EQ57905787-0B2F9FDF-F8F5-4F34-BA80-4E19C0B17743Q57905810-30ECDC2E-B07F-4C2D-A84A-311FB377F2D8Q57905812-EFA85269-D12A-4A29-8529-4514F067E17BQ57905848-FD904F47-F677-4E60-8BAD-11598F248FB0Q57906043-60704500-0733-4124-AD7F-3D93797CDC5BQ57906090-923C2B9E-BFFD-4594-838C-9FDB78DD6A83Q58092426-8513E778-94D7-4178-9D5E-59F2BBEE0C27Q58577786-7A674CD4-E8E1-4694-9464-812122F3A02EQ60457463-FB6C78E1-504A-4B54-B91E-5EDDB428EFB1Q60457465-A000BB34-FAB6-47FC-841B-51831191BFE4Q63348546-5152FD5F-ADA3-4D2D-9DBC-3F154209BCB5Q64028702-F2B22F74-DD89-4418-9D49-B55B439305C9Q79180351-A98CFE20-E04D-493A-8F7C-FFC41772C827Q79753428-0445F55D-0D9C-4E61-8889-B49542D6227FQ80764624-F33F5706-82FA-4735-9D39-D85CF1F98C4EQ82433010-E98E8740-ABA2-43A9-9E96-575018C83A8CQ84583530-40331CAB-C65F-4EAF-93F7-B9044F6972D9Q84596663-4A107D26-81F1-4D34-8C57-7F508CD36FD8Q84867920-C59F2E7A-C552-4A52-B1E9-9417D36323BEQ85027680-1DDC79DE-84AE-4B9E-985F-42BEA21BB300Q85249990-B7D4BD32-04C4-4CD4-AF79-EB6037BB4EB3
P50
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India keemik
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Indian chemist
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Indian chemist
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Indian chemist
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academicus
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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স্বাধীন কুমার মন্ডল
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin K Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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Swadhin Kumar Mandal
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স্বাধীন কুমার মন্ডল
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P69
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P2381
P27
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0000-0003-3471-7053
P551
P569
1973-01-01T00:00:00Z