VIAF

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Leader     00000nz a2200037n 45 0
001     WKP|Q45277442  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241020233022.0
008     241020nneanz||abbn n and d
035 ‎‡a  (WKP)Q45277442‏
024 ‎‡a  0000-0002-9605-3611‏ ‎‡2  orcid‏
024 ‎‡a  7401676356‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q45277442‏
100 0 ‎‡a  Felipe García‏ ‎‡9  ast‏ ‎‡9  es‏ ‎‡9  sl‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  Felipe García‏ ‎‡c  researcher ORCID: 0000-0002-9605-3611‏ ‎‡9  en‏
400 0 ‎‡a  Felipe García‏ ‎‡c  onderzoeker‏ ‎‡9  nl‏
670 ‎‡a  Author's A multi-step solvent-free mechanochemical route to indium‏
670 ‎‡a  Author's A multi-step solvent-free mechanochemical route to indium(iii) complexes‏
670 ‎‡a  Author's A one-pot synthesis to [(Me3Si)3SiSb]4; a potential precursor for Sb42-‏
670 ‎‡a  Author's An unexpected pathway in the cage opening and aggregation of P4‏
670 ‎‡a  Author's Ansa-tris‏
670 ‎‡a  Author's Ansa-tris(allyl) complexes of alkali metals: tripodal analogues of cyclopentadienyl and ansa-metallocene ligands‏
670 ‎‡a  Author's Aryl-NHC-group 13 trimethyl complexes: structural, stability and bonding insights‏
670 ‎‡a  Author's Bay-Region Functionalisation of Ar-BIAN Ligands and Their Use Within Highly Absorptive Cationic Iridium‏
670 ‎‡a  Author's Bay-Region Functionalisation of Ar-BIAN Ligands and Their Use Within Highly Absorptive Cationic Iridium(III) Dyes.‏
670 ‎‡a  Author's Completely Solvent-free Protocols to Access Phase-Pure, Metastable Metal Halide Perovskites and Functional Photodetectors from the Precursor Salts‏
670 ‎‡a  Author's Confinement of halide ions within homologous inverse coordination hosts; modification of halide-ion selectivity‏
670 ‎‡a  Author's Direct synthesis of the 1,2,3-[C6H4P...P...P]- anion, isoelectronic with the indenyl anion [C6H4CH...CH...CH]-.‏
670 ‎‡a  Author's Effective visible light-activated B-doped and B,N-codoped TiO2 photocatalysts‏
670 ‎‡a  Author's Efficient visible light-active N-doped TiO2 photocatalysts by a reproducible and controllable synthetic route‏
670 ‎‡a  Author's Enabling Mitochondrial Uptake of Lipophilic Dications Using Methylated Triphenylphosphonium Moieties‏
670 ‎‡a  Author's Encapsulation of hydride by molecular main group metal clusters: manipulating the source and coordination sphere of the interstitial ion‏
670 ‎‡a  Author's Exo-metal coordination by a tricyclic [(P(mu-N-2-NC5H4))2(mu-O)]2 dimer in [(P(mu-N-2-NC5H4))2(mu-O)]2(CuCl x (C5H5N)2)4 (2-NC5H4 = 2-pyridyl, C5H5N = pyridine).‏
670 ‎‡a  Author's Formation and structure of the [(1,2-C(6)H(4)P(2)Sb)(2)](4-) ion: implications for an extended family of isoelectronic main-group radicals‏
670 ‎‡a  Author's Highly selective epoxidation of styrene using a transition metal-aluminium‏
670 ‎‡a  Author's Highly selective epoxidation of styrene using a transition metal-aluminium(III) complex containing the [MeAl(2-py)3]- anion (2-py = 2-pyridyl).‏
670 ‎‡a  Author's Inverse coordination of an ionic lattice by a metal host‏
670 ‎‡a  Author's Main group mechanochemistry‏
670 ‎‡a  Author's Main group mechanochemistry: from curiosity to established protocols‏
670 ‎‡a  Author's Mechanochemical Synthesis of Phosphazane-Based Frameworks.‏
670 ‎‡a  Author's Mixed alkylamido aluminate as a kinetically controlled base‏
670 ‎‡a  Author's Orthogonality in main group compounds: a direct one-step synthesis of air- and moisture-stable cyclophosphazanes by mechanochemistry‏
670 ‎‡a  Author's pi-Bonding versus oligomerisation in the aromatic anions [C(6)H(4)N(2)E](-): formation of the cyclic tetrameric tetraanion [C(6)H(4)N(2)Sb](4)(4-)‏
670 ‎‡a  Author's Pyridyl 'ring-flipping' in the dimers [Me2E(2-py)]2 (E=B, Al, Ga; 2-py=2-pyridyl)‏
670 ‎‡a  Author's Quadruple deprotonation of 2-aminophenylphosphane with a p-block-metal/alkali-metal base‏
670 ‎‡a  Author's Reactions of Sn(NMe2)2 with MPHCy: The Effects of Alkali Metal Phosphide Coupling (Cy=Cyclohexyl; M=Li, Na, K, Rb)‏
670 ‎‡a  Author's Reactions of Sn(NMe2)2with Alkali-Metaltert-ButylphosphidestBuPHM (M = Li, Na, K): Evidence for Metal-Induced Modification of the Tin(II) Phosphinidene Anions‏
670 ‎‡a  Author's Reactions of Sn(NMe2)2with Primary Aryl Phosphides, ArPH-: Synthesis and Structures of the Heteroleptic Cages [{(PhP−PPh)Sn(μ-PPh)}2(Na·PMDETA)4and [{Sn(μ3-Ppy)}3{Sn(μ3,μ1-pyP−Ppy)}3]‏
670 ‎‡a  Author's Reductive-elimination of phosphide units; the basis of a general approach to a range of alloys and materials‏
670 ‎‡a  Author's Selection of a Pentameric Host in the Host-Guest Complexes {[{[P‏
670 ‎‡a  Author's Selection of a Pentameric Host in the Host-Guest Complexes {[{[P(μ-NtBu)]2(μ-NH)}5]⋅I}−[Li(thf)4]+and [{[P(μ-NtBu)]2(μ-NH)}5]⋅HBr⋅THF‏
670 ‎‡a  Author's Selection of the cis and trans phosph(iii)azane macrocycles [{P(µ-NtBu)}2(1-Y-2-NH-C6H4)]2(Y = O, S)‏
670 ‎‡a  Author's Selective formation of the [PhP(H)-PPh]- anion in the reaction of PhPHLi with MeAlCl(2); synthesis and structure of the unusual tetramer [(PhP(H)-PPh)Li.thf]4‏
670 ‎‡a  Author's Single- and double-bridged PNP ligands in chromium-catalysed ethylene oligomerisation‏
670 ‎‡a  Author's Stepwise nucleophilic substitution of manganocene, syntheses and structures of the dimer [CpMn(hpp)]2 and the unusual manganate cage [LiMn(hpp)3]2 (hppH = 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2,a]pyrimidine)‏
670 ‎‡a  Author's Steric C-N bond activation on the dimeric macrocycle [{P‏
670 ‎‡a  Author's Steric C-N bond activation on the dimeric macrocycle [{P(μ-NR)}2(μ-NR)]2.‏
670 ‎‡a  Author's Steric control in the oligomerisation of phosphazane dimers; towards new phosphorus-nitrogen macrocycles‏
670 ‎‡a  Author's Structural, Solid-State NMR and Theoretical Studies of the Inverse-Coordination of Lithium Chloride Using Group 13 Phosphide Hosts‏
670 ‎‡a  Author's Synthesis and Hydrolytic Studies on the Air-Stable [(4-CN-PhO)(E)P(μ-N(t)Bu)]2 (E = O, S, and Se) Cyclodiphosphazanes.‏
670 ‎‡a  Author's Synthesis and structure of [[MeAl(mu-PMes)(PMes)]2Li4]2 x 7thf, containing a [MeAl(mu-PMes)(PMes)]2(4-) tetraanion (Mes = 2,4,6-Me3C6H2)‏
670 ‎‡a  Author's Synthesis and Structure of [{Sn2(μ-PMes)3}K2·3THF]∞, Exhibiting Multifunctional Coordination of [Sn2(μ-PMes)3]2-Anions to K+‏
670 ‎‡a  Author's Synthesis and structure of the calixarene-like phosph(III)azane macrocycle [{P(mu-N(t)Bu)}2{1,5-(NH)2C10H6}]3.‏
670 ‎‡a  Author's Synthesis and structure of the Li13 cage [{[OP(μ-NtBu)]2Li2}3(LiCl)6Li(Cl/OnBu)0.5(thf)7], containing a [OP(μ-NtBu)]22− dianion‏
670 ‎‡a  Author's Synthesis and the Optical and Electrochemical Properties of Indium‏
670 ‎‡a  Author's Synthesis and the Optical and Electrochemical Properties of Indium(III) Bis(arylimino)acenaphthene Complexes.‏
670 ‎‡a  Author's Synthesis of a deca-lithium cage containing an [‏
670 ‎‡a  Author's Synthesis of a deca-lithium cage containing an [(RN)2As(mu-NR)As(NR)2]4- tetraanion; a homologue of group 15 trianions of the type [E(NR)3]3-.‏
670 ‎‡a  Author's Synthesis of Unique Phosphazane Macrocycles via Steric Activation of C-N Bonds‏
670 ‎‡a  Author's Synthesis, structural studies and ligand influence on the stability of aryl-NHC stabilised trimethylaluminium complexes.‏
670 ‎‡a  Author's Targeting large phosp(III)azane macrocyles [{P(mu-NR)}(2)(LL)](n) (n> or = 2)‏
670 ‎‡a  Author's Templating and selection in the formation of macrocycles containing [[P‏
670 ‎‡a  Author's Templating and selection in the formation of macrocycles containing [[P(micro-NtBu)(2)](micro-NH)](n) frameworks: observation of halide ion coordination‏
670 ‎‡a  Author's The cationic cluster Grignard [{MgCl‏
670 ‎‡a  Author's The cationic cluster Grignard [{MgCl(thf)2}3(μ3-C3H5)2]+‏
670 ‎‡a  Author's The first example of a Si-bridged tris(pyridyl) ligand; synthesis and structure of [MeSi(2-C5H4N)3LiX](X = 0.2Br, 0.8Cl)‏
670 ‎‡a  Author's The First Synthesis of the Sterically Encumbered Adamantoid Phosphazane P4‏
670 ‎‡a  Author's The First Synthesis of the Sterically Encumbered Adamantoid Phosphazane P4 (N(t) Bu)6 : Enabled by Mechanochemistry‏
670 ‎‡a  Author's The folded, tetrameric phosph(III)azane macrocycle [(P(mu-NtBu))2(1,4-(NH)2C6H4)]4.‏
670 ‎‡a  Author's The formation of dimeric phosph(III)azane macrocycles [[P(mu-NtBu)]2.LL]2 [LL = organic spacer]‏
670 ‎‡a  Author's thermodynamic/kinetic control in the isomerization of the [[tBuNP(mu-NtBu)]2]2- ion‏
670 ‎‡a  Author's Trapping of oligomeric cyclopentadienyllithium cationic and anionic fragments by a V[triple bond]V-bonded ligand‏
670 ‎‡a  Author's Triphosph(III)azanes to diphosph(III)azanes; a cracking transformation‏
670 ‎‡a  Author's Unique Triphenylphosphonium Derivatives for Enhanced Mitochondrial Uptake and Photodynamic Therapy.‏
909 ‎‡a  (scopus) 7401676356‏ ‎‡9  1‏
909 ‎‡a  (orcid) 0000000296053611‏ ‎‡9  1‏
919 ‎‡a  multistepsolventfreemechanochemicalroutetoindium3complexes‏ ‎‡A  A multi-step solvent-free mechanochemical route to indium(iii) complexes‏ ‎‡9  1‏
919 ‎‡a  multistepsolventfreemechanochemicalroutetoindium‏ ‎‡A  A multi-step solvent-free mechanochemical route to indium‏ ‎‡9  1‏
919 ‎‡a  uniquetriphenylphosphoniumderivativesforenhancedmitochondrialuptakeandphotodynamictherapy‏ ‎‡A  Unique Triphenylphosphonium Derivatives for Enhanced Mitochondrial Uptake and Photodynamic Therapy.‏ ‎‡9  1‏
919 ‎‡a  triphosph3azanestodiphosph3azanesacrackingtransformation‏ ‎‡A  Triphosph(III)azanes to diphosph(III)azanes; a cracking transformation‏ ‎‡9  1‏
919 ‎‡a  trappingofoligomericcyclopentadienyllithiumcationicandanionicfragmentsbyavvbondedligand‏ ‎‡A  Trapping of oligomeric cyclopentadienyllithium cationic and anionic fragments by a V[triple bond]V-bonded ligand‏ ‎‡9  1‏
919 ‎‡a  thermodynamickineticcontrolintheisomerizationofthe2ion‏ ‎‡A  thermodynamic/kinetic control in the isomerization of the [[tBuNP(mu-NtBu)]2]2- ion‏ ‎‡9  1‏
919 ‎‡a  formationofdimericphosph3azanemacrocycles2‏ ‎‡A  The formation of dimeric phosph(III)azane macrocycles [[P(mu-NtBu)]2.LL]2 [LL = organic spacer]‏ ‎‡9  1‏
919 ‎‡a  foldedtetramericphosph3azanemacrocycle4‏ ‎‡A  The folded, tetrameric phosph(III)azane macrocycle [(P(mu-NtBu))2(1,4-(NH)2C6H4)]4.‏ ‎‡9  1‏
919 ‎‡a  1synthesisofthestericallyencumberedadamantoidphosphazanep4ntbu6enabledbymechanochemistry‏ ‎‡A  The First Synthesis of the Sterically Encumbered Adamantoid Phosphazane P4 (N(t) Bu)6 : Enabled by Mechanochemistry‏ ‎‡9  1‏
919 ‎‡a  1synthesisofthestericallyencumberedadamantoidphosphazanep4‏ ‎‡A  The First Synthesis of the Sterically Encumbered Adamantoid Phosphazane P4‏ ‎‡9  1‏
919 ‎‡a  1exampleofasibridgedtrispyridylligandsynthesisandstructureof1002br08cl‏ ‎‡A  The first example of a Si-bridged tris(pyridyl) ligand; synthesis and structure of [MeSi(2-C5H4N)3LiX](X = 0.2Br, 0.8Cl)‏ ‎‡9  1‏
919 ‎‡a  cationicclustergrignard+‏ ‎‡A  The cationic cluster Grignard [{MgCl(thf)2}3(μ3-C3H5)2]+‏ ‎‡9  1‏
919 ‎‡a  cationicclustergrignardmgcl‏ ‎‡A  The cationic cluster Grignard [{MgCl‏ ‎‡9  1‏
919 ‎‡a  templatingandselectionintheformationofmacrocyclescontainingnframeworksobservationofhalideioncoordination‏ ‎‡A  Templating and selection in the formation of macrocycles containing [[P(micro-NtBu)(2)](micro-NH)](n) frameworks: observation of halide ion coordination‏ ‎‡9  1‏
919 ‎‡a  templatingandselectionintheformationofmacrocyclescontainingp‏ ‎‡A  Templating and selection in the formation of macrocycles containing [[P‏ ‎‡9  1‏
919 ‎‡a  targetinglargephosp3azanemacrocylesnnor2‏ ‎‡A  Targeting large phosp(III)azane macrocyles [{P(mu-NR)}(2)(LL)](n) (n> or = 2)‏ ‎‡9  1‏
919 ‎‡a  synthesisstructuralstudiesandligandinfluenceonthestabilityofarylnhcstabilisedtrimethylaluminiumcomplexes‏ ‎‡A  Synthesis, structural studies and ligand influence on the stability of aryl-NHC stabilised trimethylaluminium complexes.‏ ‎‡9  1‏
919 ‎‡a  synthesisofuniquephosphazanemacrocyclesviastericactivationof100nbonds‏ ‎‡A  Synthesis of Unique Phosphazane Macrocycles via Steric Activation of C-N Bonds‏ ‎‡9  1‏
919 ‎‡a  synthesisofadecalithiumcagecontainingan4tetraanionahomologueofgroup15trianionsofthetype3‏ ‎‡A  Synthesis of a deca-lithium cage containing an [(RN)2As(mu-NR)As(NR)2]4- tetraanion; a homologue of group 15 trianions of the type [E(NR)3]3-.‏ ‎‡9  1‏
919 ‎‡a  synthesisofadecalithiumcagecontainingan‏ ‎‡A  Synthesis of a deca-lithium cage containing an [‏ ‎‡9  1‏
919 ‎‡a  synthesisandtheopticalandelectrochemicalpropertiesofindium3bisaryliminoacenaphthenecomplexes‏ ‎‡A  Synthesis and the Optical and Electrochemical Properties of Indium(III) Bis(arylimino)acenaphthene Complexes.‏ ‎‡9  1‏
919 ‎‡a  synthesisandtheopticalandelectrochemicalpropertiesofindium‏ ‎‡A  Synthesis and the Optical and Electrochemical Properties of Indium‏ ‎‡9  1‏
919 ‎‡a  synthesisandstructureoftheli13cagecontaininga22dianion‏ ‎‡A  Synthesis and structure of the Li13 cage [{[OP(μ-NtBu)]2Li2}3(LiCl)6Li(Cl/OnBu)0.5(thf)7], containing a [OP(μ-NtBu)]22− dianion‏ ‎‡9  1‏
919 ‎‡a  synthesisandstructureofthecalixarenelikephosph3azanemacrocycle3‏ ‎‡A  Synthesis and structure of the calixarene-like phosph(III)azane macrocycle [{P(mu-N(t)Bu)}2{1,5-(NH)2C10H6}]3.‏ ‎‡9  1‏
919 ‎‡a  synthesisandstructureofexhibitingmultifunctionalcoordinationof2anionstok+‏ ‎‡A  Synthesis and Structure of [{Sn2(μ-PMes)3}K2·3THF]∞, Exhibiting Multifunctional Coordination of [Sn2(μ-PMes)3]2-Anions to K+‏ ‎‡9  1‏
919 ‎‡a  synthesisandstructureof2107thfcontaininga24tetraanionmes246me3c6h2‏ ‎‡A  Synthesis and structure of [[MeAl(mu-PMes)(PMes)]2Li4]2 x 7thf, containing a [MeAl(mu-PMes)(PMes)]2(4-) tetraanion (Mes = 2,4,6-Me3C6H2)‏ ‎‡9  1‏
919 ‎‡a  synthesisandhydrolyticstudiesontheairstable2eosandsecyclodiphosphazanes‏ ‎‡A  Synthesis and Hydrolytic Studies on the Air-Stable [(4-CN-PhO)(E)P(μ-N(t)Bu)]2 (E = O, S, and Se) Cyclodiphosphazanes.‏ ‎‡9  1‏
919 ‎‡a  structuralsolidstatenmrandtheoreticalstudiesoftheinversecoordinationoflithiumchlorideusinggroup13phosphidehosts‏ ‎‡A  Structural, Solid-State NMR and Theoretical Studies of the Inverse-Coordination of Lithium Chloride Using Group 13 Phosphide Hosts‏ ‎‡9  1‏
919 ‎‡a  stericcontrolintheoligomerisationofphosphazanedimerstowardsnewphosphorusnitrogenmacrocycles‏ ‎‡A  Steric control in the oligomerisation of phosphazane dimers; towards new phosphorus-nitrogen macrocycles‏ ‎‡9  1‏
919 ‎‡a  steric100nbondactivationonthedimericmacrocycle2‏ ‎‡A  Steric C-N bond activation on the dimeric macrocycle [{P(μ-NR)}2(μ-NR)]2.‏ ‎‡9  1‏
919 ‎‡a  steric100nbondactivationonthedimericmacrocyclep‏ ‎‡A  Steric C-N bond activation on the dimeric macrocycle [{P‏ ‎‡9  1‏
919 ‎‡a  stepwisenucleophilicsubstitutionofmanganocenesynthesesandstructuresofthedimer2andtheunusualmanganatecage2hpph134678hexahydro2hpyrimidopyrimidine‏ ‎‡A  Stepwise nucleophilic substitution of manganocene, syntheses and structures of the dimer [CpMn(hpp)]2 and the unusual manganate cage [LiMn(hpp)3]2 (hppH = 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2,a]pyrimidine)‏ ‎‡9  1‏
919 ‎‡a  singleanddoublebridgedpnpligandsinchromiumcatalysedethyleneoligomerisation‏ ‎‡A  Single- and double-bridged PNP ligands in chromium-catalysed ethylene oligomerisation‏ ‎‡9  1‏
919 ‎‡a  selectiveformationoftheanioninthereactionofphphliwithmealcl2synthesisandstructureoftheunusualtetramer4‏ ‎‡A  Selective formation of the [PhP(H)-PPh]- anion in the reaction of PhPHLi with MeAlCl(2); synthesis and structure of the unusual tetramer [(PhP(H)-PPh)Li.thf]4‏ ‎‡9  1‏
919 ‎‡a  selectionofthecisandtransphosph3azanemacrocycles2yos‏ ‎‡A  Selection of the cis and trans phosph(iii)azane macrocycles [{P(µ-NtBu)}2(1-Y-2-NH-C6H4)]2(Y = O, S)‏ ‎‡9  1‏
919 ‎‡a  selectionofapentamerichostinthehostguestcomplexes1+andhbrthf‏ ‎‡A  Selection of a Pentameric Host in the Host-Guest Complexes {[{[P(μ-NtBu)]2(μ-NH)}5]⋅I}−[Li(thf)4]+and [{[P(μ-NtBu)]2(μ-NH)}5]⋅HBr⋅THF‏ ‎‡9  1‏
919 ‎‡a  selectionofapentamerichostinthehostguestcomplexesp‏ ‎‡A  Selection of a Pentameric Host in the Host-Guest Complexes {[{[P‏ ‎‡9  1‏
919 ‎‡a  reductiveeliminationofphosphideunitsthebasisofageneralapproachtoarangeofalloysandmaterials‏ ‎‡A  Reductive-elimination of phosphide units; the basis of a general approach to a range of alloys and materials‏ ‎‡9  1‏
919 ‎‡a  reactionsofsnnme22withprimaryarylphosphidesarphsynthesisandstructuresoftheheterolepticcagesphppphsnμpph2napmdeta4and‏ ‎‡A  Reactions of Sn(NMe2)2with Primary Aryl Phosphides, ArPH-: Synthesis and Structures of the Heteroleptic Cages [{(PhP−PPh)Sn(μ-PPh)}2(Na·PMDETA)4and [{Sn(μ3-Ppy)}3{Sn(μ3,μ1-pyP−Ppy)}3]‏ ‎‡9  1‏
919 ‎‡a  reactionsofsnnme22withalkalimetaltertbutylphosphidestbuphm100051nakevidenceformetalinducedmodificationofthetin2phosphinideneanions‏ ‎‡A  Reactions of Sn(NMe2)2with Alkali-Metaltert-ButylphosphidestBuPHM (M = Li, Na, K): Evidence for Metal-Induced Modification of the Tin(II) Phosphinidene Anions‏ ‎‡9  1‏
919 ‎‡a  reactionsofsnnme22withmphcytheeffectsofalkalimetalphosphidecouplingcycyclohexyl100051nakrb‏ ‎‡A  Reactions of Sn(NMe2)2 with MPHCy: The Effects of Alkali Metal Phosphide Coupling (Cy=Cyclohexyl; M=Li, Na, K, Rb)‏ ‎‡9  1‏
919 ‎‡a  quadrupledeprotonationof2aminophenylphosphanewithapblockmetalalkalimetalbase‏ ‎‡A  Quadruple deprotonation of 2-aminophenylphosphane with a p-block-metal/alkali-metal base‏ ‎‡9  1‏
919 ‎‡a  pyridylringflippinginthedimers2ebalga2py2pyridyl‏ ‎‡A  Pyridyl 'ring-flipping' in the dimers [Me2E(2-py)]2 (E=B, Al, Ga; 2-py=2-pyridyl)‏ ‎‡9  1‏
919 ‎‡a  pibondingversusoligomerisationinthearomaticanionsformationofthecyclictetramerictetraanion44‏ ‎‡A  pi-Bonding versus oligomerisation in the aromatic anions [C(6)H(4)N(2)E](-): formation of the cyclic tetrameric tetraanion [C(6)H(4)N(2)Sb](4)(4-)‏ ‎‡9  1‏
919 ‎‡a  orthogonalityinmaingroupcompoundsadirect1stepsynthesisofairandmoisturestablecyclophosphazanesbymechanochemistry‏ ‎‡A  Orthogonality in main group compounds: a direct one-step synthesis of air- and moisture-stable cyclophosphazanes by mechanochemistry‏ ‎‡9  1‏
919 ‎‡a  mixedalkylamidoaluminateasakineticallycontrolledbase‏ ‎‡A  Mixed alkylamido aluminate as a kinetically controlled base‏ ‎‡9  1‏
919 ‎‡a  mechanochemicalsynthesisofphosphazanebasedframeworks‏ ‎‡A  Mechanochemical Synthesis of Phosphazane-Based Frameworks.‏ ‎‡9  1‏
919 ‎‡a  maingroupmechanochemistryfromcuriositytoestablishedprotocols‏ ‎‡A  Main group mechanochemistry: from curiosity to established protocols‏ ‎‡9  1‏
919 ‎‡a  maingroupmechanochemistry‏ ‎‡A  Main group mechanochemistry‏ ‎‡9  1‏
919 ‎‡a  inversecoordinationofanioniclatticebyametalhost‏ ‎‡A  Inverse coordination of an ionic lattice by a metal host‏ ‎‡9  1‏
919 ‎‡a  highlyselectiveepoxidationofstyreneusingatransitionmetalaluminium3complexcontainingtheanion2py2pyridyl‏ ‎‡A  Highly selective epoxidation of styrene using a transition metal-aluminium(III) complex containing the [MeAl(2-py)3]- anion (2-py = 2-pyridyl).‏ ‎‡9  1‏
919 ‎‡a  highlyselectiveepoxidationofstyreneusingatransitionmetalaluminium‏ ‎‡A  Highly selective epoxidation of styrene using a transition metal-aluminium‏ ‎‡9  1‏
919 ‎‡a  formationandstructureofthe4ionimplicationsforanextendedfamilyofisoelectronicmaingroupradicals‏ ‎‡A  Formation and structure of the [(1,2-C(6)H(4)P(2)Sb)(2)](4-) ion: implications for an extended family of isoelectronic main-group radicals‏ ‎‡9  1‏
919 ‎‡a  exometalcoordinationbyatricyclic2dimerin2cucl10c5h5n242nc5h42pyridylc5h5npyridine‏ ‎‡A  Exo-metal coordination by a tricyclic [(P(mu-N-2-NC5H4))2(mu-O)]2 dimer in [(P(mu-N-2-NC5H4))2(mu-O)]2(CuCl x (C5H5N)2)4 (2-NC5H4 = 2-pyridyl, C5H5N = pyridine).‏ ‎‡9  1‏
919 ‎‡a  encapsulationofhydridebymolecularmaingroupmetalclustersmanipulatingthesourceandcoordinationsphereoftheinterstitialion‏ ‎‡A  Encapsulation of hydride by molecular main group metal clusters: manipulating the source and coordination sphere of the interstitial ion‏ ‎‡9  1‏
919 ‎‡a  enablingmitochondrialuptakeoflipophilicdicationsusingmethylatedtriphenylphosphoniummoieties‏ ‎‡A  Enabling Mitochondrial Uptake of Lipophilic Dications Using Methylated Triphenylphosphonium Moieties‏ ‎‡9  1‏
919 ‎‡a  efficientvisiblelightactivendopedtio2photocatalystsbyareproducibleandcontrollablesyntheticroute‏ ‎‡A  Efficient visible light-active N-doped TiO2 photocatalysts by a reproducible and controllable synthetic route‏ ‎‡9  1‏
919 ‎‡a  effectivevisiblelightactivatedbdopedandbncodopedtio2photocatalysts‏ ‎‡A  Effective visible light-activated B-doped and B,N-codoped TiO2 photocatalysts‏ ‎‡9  1‏
919 ‎‡a  directsynthesisofthe123anionisoelectronicwiththeindenylanion‏ ‎‡A  Direct synthesis of the 1,2,3-[C6H4P...P...P]- anion, isoelectronic with the indenyl anion [C6H4CH...CH...CH]-.‏ ‎‡9  1‏
919 ‎‡a  confinementofhalideionswithinhomologousinversecoordinationhostsmodificationofhalideionselectivity‏ ‎‡A  Confinement of halide ions within homologous inverse coordination hosts; modification of halide-ion selectivity‏ ‎‡9  1‏
919 ‎‡a  completelysolventfreeprotocolstoaccessphasepuremetastablemetalhalideperovskitesandfunctionalphotodetectorsfromtheprecursorsalts‏ ‎‡A  Completely Solvent-free Protocols to Access Phase-Pure, Metastable Metal Halide Perovskites and Functional Photodetectors from the Precursor Salts‏ ‎‡9  1‏
919 ‎‡a  bayregionfunctionalisationofarbianligandsandtheirusewithinhighlyabsorptivecationiciridium3dyes‏ ‎‡A  Bay-Region Functionalisation of Ar-BIAN Ligands and Their Use Within Highly Absorptive Cationic Iridium(III) Dyes.‏ ‎‡9  1‏
919 ‎‡a  bayregionfunctionalisationofarbianligandsandtheirusewithinhighlyabsorptivecationiciridium‏ ‎‡A  Bay-Region Functionalisation of Ar-BIAN Ligands and Their Use Within Highly Absorptive Cationic Iridium‏ ‎‡9  1‏
919 ‎‡a  arylnhcgroup13trimethylcomplexesstructuralstabilityandbondinginsights‏ ‎‡A  Aryl-NHC-group 13 trimethyl complexes: structural, stability and bonding insights‏ ‎‡9  1‏
919 ‎‡a  ansatrisallylcomplexesofalkalimetalstripodalanaloguesofcyclopentadienylandansametalloceneligands‏ ‎‡A  Ansa-tris(allyl) complexes of alkali metals: tripodal analogues of cyclopentadienyl and ansa-metallocene ligands‏ ‎‡9  1‏
919 ‎‡a  ansatris‏ ‎‡A  Ansa-tris‏ ‎‡9  1‏
919 ‎‡a  unexpectedpathwayinthecageopeningandaggregationofp4‏ ‎‡A  An unexpected pathway in the cage opening and aggregation of P4‏ ‎‡9  1‏
919 ‎‡a  1potsynthesisto4apotentialprecursorforsb42‏ ‎‡A  A one-pot synthesis to [(Me3Si)3SiSb]4; a potential precursor for Sb42-‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
996 ‎‡2  ISNI|000000013890525X‏
996 ‎‡2  BNE|XX1660850‏
996 ‎‡2  BNE|XX1130930‏
996 ‎‡2  ISNI|0000000431424375‏
996 ‎‡2  DNB|1057684511‏
996 ‎‡2  ISNI|0000000079707682‏
996 ‎‡2  LC|no2020150562‏
996 ‎‡2  ISNI|0000000031945147‏
996 ‎‡2  NTA|352060239‏
996 ‎‡2  BIBSYS|90066529‏
996 ‎‡2  SUDOC|259945013‏
996 ‎‡2  BNE|XX1319953‏
996 ‎‡2  SUDOC|24206437X‏
996 ‎‡2  LC|ns2022001309‏
996 ‎‡2  LC|n 88024889‏
996 ‎‡2  NUKAT|n 2016177349‏
996 ‎‡2  DNB|1329648730‏
996 ‎‡2  ISNI|0000000059345338‏
996 ‎‡2  BNE|XX1123236‏
996 ‎‡2  BLBNB|001569360‏
996 ‎‡2  BNF|18062829‏
996 ‎‡2  ISNI|0000000078290993‏
996 ‎‡2  SUDOC|119826127‏
996 ‎‡2  LC|no2007058987‏
996 ‎‡2  BNE|XX972601‏
996 ‎‡2  PTBNP|1919430‏
996 ‎‡2  ISNI|0000000071994875‏
996 ‎‡2  BNE|XX1598110‏
996 ‎‡2  LC|n 2024253719‏
996 ‎‡2  SUDOC|195000218‏
996 ‎‡2  BNE|XX925145‏
996 ‎‡2  BNE|XX1755023‏
996 ‎‡2  BNC|981060557262806706‏
996 ‎‡2  BNE|XX1723523‏
996 ‎‡2  LC|nr 91015557‏
996 ‎‡2  BNE|XX1543102‏
996 ‎‡2  ISNI|0000000108563201‏
996 ‎‡2  LC|no 96016700‏
996 ‎‡2  ISNI|0000000459717751‏
996 ‎‡2  BNC|981058525099106706‏
996 ‎‡2  BIBSYS|8000892‏
996 ‎‡2  DNB|130413496‏
996 ‎‡2  BNF|14966066‏
996 ‎‡2  ISNI|000000007973447X‏
996 ‎‡2  PTBNP|1531396‏
996 ‎‡2  BNF|14180166‏
996 ‎‡2  ISNI|0000000118669421‏
996 ‎‡2  BNE|XX4959860‏
996 ‎‡2  J9U|987007334729805171‏
996 ‎‡2  SUDOC|170512932‏
996 ‎‡2  LC|n 2017072536‏
996 ‎‡2  BNF|14180165‏
996 ‎‡2  NII|DA18802953‏
996 ‎‡2  DNB|1056506660‏
996 ‎‡2  ISNI|0000000059370453‏
996 ‎‡2  RERO|A018406115‏
996 ‎‡2  ISNI|0000000068491433‏
996 ‎‡2  LC|no2008077155‏
996 ‎‡2  LC|n 2013019193‏
996 ‎‡2  ISNI|0000000078274248‏
996 ‎‡2  ISNI|0000000447250509‏
996 ‎‡2  LC|n 2015012129‏
996 ‎‡2  DNB|1237285267‏
996 ‎‡2  BNE|XX5297599‏
996 ‎‡2  BNE|XX1240914‏
996 ‎‡2  RERO|A012704881‏
996 ‎‡2  LC|no2013015856‏
996 ‎‡2  NUKAT|n 2015178769‏
996 ‎‡2  DNB|13520898X‏
996 ‎‡2  BNC|981058611900906706‏
996 ‎‡2  LC|n 00000682‏
996 ‎‡2  BNE|XX871507‏
996 ‎‡2  NKC|mzk2013750816‏
996 ‎‡2  ISNI|0000000108613280‏
996 ‎‡2  SUDOC|225532441‏
996 ‎‡2  PTBNP|1327969‏
996 ‎‡2  BNC|981058616613306706‏
996 ‎‡2  BNE|XX1062923‏
996 ‎‡2  ISNI|0000000464201047‏
996 ‎‡2  SUDOC|164907505‏
996 ‎‡2  SUDOC|106927132‏
996 ‎‡2  SUDOC|271681209‏
996 ‎‡2  BNE|XX5001190‏
996 ‎‡2  BNE|XX1100950‏
996 ‎‡2  BNC|981058517326606706‏
996 ‎‡2  LC|n 2001098640‏
996 ‎‡2  LC|no2002025691‏
996 ‎‡2  ISNI|0000000068246622‏
996 ‎‡2  BNE|XX1554501‏
996 ‎‡2  VLACC|000043612‏
996 ‎‡2  LC|n 79070137‏
996 ‎‡2  LC|n 86853667‏
996 ‎‡2  ISNI|0000000509873710‏
996 ‎‡2  RERO|A011473527‏
996 ‎‡2  ISNI|0000000500964544‏
996 ‎‡2  SUDOC|137700903‏
996 ‎‡2  DNB|1053949189‏
996 ‎‡2  BIBSYS|1065389‏
996 ‎‡2  BNE|XX831266‏
996 ‎‡2  ISNI|0000000079916257‏
996 ‎‡2  LC|nr 96024798‏
996 ‎‡2  BNCHL|10000000000000000825912‏
996 ‎‡2  BNF|17087874‏
996 ‎‡2  BNE|XX1398872‏
996 ‎‡2  DNB|1026456940‏
996 ‎‡2  ISNI|0000000140358312‏
996 ‎‡2  BIBSYS|12019311‏
996 ‎‡2  BNE|XX1536225‏
996 ‎‡2  LC|no2009135643‏
996 ‎‡2  BNC|981058515380206706‏
996 ‎‡2  DNB|1122058381‏
996 ‎‡2  JPG|500341319‏
996 ‎‡2  B2Q|0000842057‏
996 ‎‡2  LC|n 2011044304‏
996 ‎‡2  B2Q|0001243609‏
996 ‎‡2  ISNI|0000000047468787‏
996 ‎‡2  SUDOC|268389454‏
996 ‎‡2  SUDOC|147597749‏
996 ‎‡2  VLACC|000043613‏
996 ‎‡2  SUDOC|136481655‏
996 ‎‡2  ISNI|0000000059406428‏
996 ‎‡2  DNB|122113330‏
996 ‎‡2  ISNI|0000000024978653‏
996 ‎‡2  ISNI|0000000070205176‏
996 ‎‡2  ISNI|0000000080904595‏
996 ‎‡2  BNCHL|10000000000000000833708‏
996 ‎‡2  SUDOC|127856064‏
996 ‎‡2  ISNI|0000000059655838‏
996 ‎‡2  LC|no2002053320‏
996 ‎‡2  SUDOC|232423741‏
996 ‎‡2  BNCHL|10000000000000000840083‏
996 ‎‡2  ISNI|0000000401772782‏
996 ‎‡2  BNE|XX5559725‏
996 ‎‡2  ISNI|0000000416602743‏
996 ‎‡2  NII|DA12841715‏
996 ‎‡2  LC|ns2020001048‏
996 ‎‡2  BNE|XX5774445‏
996 ‎‡2  ISNI|0000000048204484‏
996 ‎‡2  BNE|XX4665222‏
996 ‎‡2  BNF|17704854‏
996 ‎‡2  BNC|981058612183206706‏
996 ‎‡2  BNCHL|10000000000000000258853‏
996 ‎‡2  ARBABN|000026983‏
996 ‎‡2  NII|DA09714979‏
996 ‎‡2  LC|n 97105828‏
996 ‎‡2  PTBNP|1482336‏
996 ‎‡2  BNC|981058594904906706‏
996 ‎‡2  PTBNP|157080‏
996 ‎‡2  DNB|1057368490‏
996 ‎‡2  BNE|XX4832140‏
996 ‎‡2  LC|n 2020180342‏
996 ‎‡2  ISNI|0000000042337710‏
996 ‎‡2  LC|n 00098854‏
996 ‎‡2  LC|no2007008170‏
996 ‎‡2  LC|n 95027193‏
996 ‎‡2  LC|no2018033498‏
996 ‎‡2  ARBABN|000062312‏
996 ‎‡2  SUDOC|26534347X‏
996 ‎‡2  LC|n 2006063100‏
996 ‎‡2  DNB|141697466‏
996 ‎‡2  BNE|XX959880‏
996 ‎‡2  BNE|XX1169135‏
996 ‎‡2  ISNI|0000000025767479‏
996 ‎‡2  DNB|1031146547‏
996 ‎‡2  DNB|104792577X‏
996 ‎‡2  BNE|XX1030317‏
996 ‎‡2  LC|no2016039107‏
996 ‎‡2  ISNI|0000000053338225‏
996 ‎‡2  SUDOC|087269988‏
996 ‎‡2  PTBNP|88650‏
996 ‎‡2  ISNI|0000000120800302‏
996 ‎‡2  BNC|981058601449006706‏
996 ‎‡2  BNF|17071697‏
996 ‎‡2  SUDOC|138533016‏
996 ‎‡2  BNF|16170001‏
996 ‎‡2  LC|n 2015012718‏
996 ‎‡2  PTBNP|1257965‏
996 ‎‡2  NKC|pna20231201929‏
996 ‎‡2  LC|no2002071112‏
996 ‎‡2  CAOONL|ncf12074933‏
996 ‎‡2  BNE|XX5649369‏
996 ‎‡2  PLWABN|9814000772505606‏
996 ‎‡2  CAOONL|ncf10853769‏
996 ‎‡2  J9U|987007337510705171‏
996 ‎‡2  LC|no 97054652‏
996 ‎‡2  ISNI|0000000110230107‏
996 ‎‡2  SUDOC|151842817‏
996 ‎‡2  DNB|1057170445‏
996 ‎‡2  RERO|A025639553‏
996 ‎‡2  LC|no2015104759‏
996 ‎‡2  RERO|A009004598‏
996 ‎‡2  ISNI|0000000410039945‏
996 ‎‡2  BNC|981061194958506706‏
996 ‎‡2  RERO|A003279499‏
996 ‎‡2  BNC|981061102542406706‏
996 ‎‡2  SZ|1017911428‏
996 ‎‡2  W2Z|12019311‏
996 ‎‡2  BNF|17034942‏
996 ‎‡2  BNE|XX1052247‏
996 ‎‡2  LC|no2019182273‏
996 ‎‡2  ISNI|0000000402591836‏
996 ‎‡2  PTBNP|1331080‏
996 ‎‡2  RERO|A008743239‏
996 ‎‡2  ISNI|0000000459785084‏
996 ‎‡2  RERO|A026095107‏
996 ‎‡2  RERO|A012053752‏
996 ‎‡2  NLA|000035378052‏
996 ‎‡2  CAOONL|ncf10390557‏
996 ‎‡2  LC|ns2012002523‏
996 ‎‡2  BNE|XX911099‏
996 ‎‡2  SUDOC|233488197‏
996 ‎‡2  SUDOC|252940121‏
996 ‎‡2  SUDOC|192834142‏
996 ‎‡2  BNC|981058514935806706‏
996 ‎‡2  DNB|1017911428‏
996 ‎‡2  BNE|XX4758479‏
996 ‎‡2  PLWABN|9810689535905606‏
996 ‎‡2  ISNI|0000000074088237‏
996 ‎‡2  SUDOC|153252243‏
996 ‎‡2  DNB|1057247340‏
996 ‎‡2  BNE|XX1320490‏
996 ‎‡2  BNCHL|10000000000000000825954‏
996 ‎‡2  ISNI|0000000081477273‏
996 ‎‡2  ISNI|0000000513532193‏
996 ‎‡2  BNF|12384917‏
996 ‎‡2  BNE|XX1360734‏
996 ‎‡2  DNB|1219170135‏
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏
998 ‎‡a  García, Felipe‏ ‎‡c  (Chemist)‏ ‎‡2  LC|n 2023016030‏ ‎‡3  standard number‏