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- 1 5
- 1-10-Phenantroline-5-6-dione 1
- 13C CP MAS NMR Spectroscopy 1
- 1 3-Thiazolidinedione 1
- 1-phenylpiperazine 2
- 1-Thiophen-2-yl-3-thiophen-3-ylpropane-1 1
- 2 1
- 23-dihydrobenzofuran 1
- 2 3-Dihydrothiophene 1
- 2′6′4-Terpyridine 1
- 29Si MAS NMR 1
- 2-a-N-heterocycles 1
- 2D NMR 1
- 2-Mercaptoacrylic acids 1
- 2-methylbenzylamine 1
- 2-Phenylquinoline 1
- 2-Spiropiperidines 1
- 2-Thenoyltrifluoroacetonate 1
- 2-thenoyltrifluoroacetone 1
- 2-Thenoyltrifluoroacetone 1
- 31P MAS NMR 1
- 3+2 cycloaddition 1
- 3-bpyrazines 1
- 3D Cells Viability 1
- 3-dialkylimidazolinium salts 1
- 3-dihydrobenzofurans 1
- 3-dione 2
- 3-Dioxolane 1
- 3 Dipolar cycloaddition 1
- 3-methylbenzylamine 1
- 46-dinitrobenzimidazole 1
- 4-amino-6-nitrobenzimidazoles 1
- 4′-bipyridine ligand 1
- 4-Diethynylbenzene-Bridged CpdppeFen+ Units Effect of 2 1
- 4-Dimethylaminopyridine 1
- 4H-Pyran 1
- 4-member ring 1
- 4-Nitrothiophenol 1
- 5-apyrimidines 1
- 5-Arylidene rhodanine 1
- 5-BENZENETETRACARBOXYLIC ACID 1
- 5-Benzodiazepine 1
- 5-Ethynyl Groups on the Chemical and Electronic Properties 1
- 71Ga 1
- 77Se MAS NMR 1
- 7-azaindole 1
- 7Li and 31P MAS NMR 1
- 7Li EXSY NMR 1
- 8-TETRACYANOQUINODIMETHANE 1
- Ab initio calculation 1
- Ab initio calculations 8
- Ab Initio Calculations 1
- Acceptor molecules 1
- ACETYLIDE COMPLEXES 1
- Acetylides 2
- A Chalcogenide 1
- ACID 1
- Acid anhydride 1
- Acide de Brønsted 1
- Acidification 1
- Acid inhibition 1
- Acidity 3
- Acids/chemistry 1
- Acridin 1
- Acridine 1
- Acridone 1
- Acrylonitrile hydrophosphination 1
- Actinide alloys and compounds 2
- Activation 1
- Activation analysis 2
- Acylsilanes 1
- Adamantane 1
- Adduct formation 1
- Adsorption 3
- Adsorption isotherms 1
- Aerobic oxidative coupling 1
- A Functional materials 1
- Ageing 1
- Aggregation induced emission 1
- Aggregation-induced emission 1
- A Glasses 1
- Ag nanoparticle 1
- Agostic 1
- Agostic bonding 1
- Agostic interactions 3
- AIM 8
- A Intermetallic compounds 1
- A Intermetallics aluminide 1
- Alachlor 1
- AlCl3-mediated reaction 1
- Alcohols 2
- Alcoholysis 1
- Aldehyde prepn ester selective redn NHC Iron Complex catalysis 1
- Aldehydes 2
- Aldol reactions 1
- Aldols 1
- ALIE 1
- Alkali metal base 1
- Alkaline earth metals 4
- Alkaline-earth metals 3
- Alkaline earths 2
- Alkaloids 2
- Alkaloids/chemical synthesis 1
- Alkaloids/chemistry 1
- Alkene hydroboration 1
- Alkenes 2
- Alkoxide ligands 1
- Alkylation 1
- Alkyl sulfonate 1
- Alkyne 1
- Alkynes 3
- Alkynyl complexes 1
- Allelopathic activity 1
- Allylic compounds 3
- Allyl ketones 1
- Alpha-Amino acid 1
- Alpha-Aminonitrile 1
- Alpha-deprotometallation 1
- Aluminium 1
- Aluminum 3
- Aluminum chloride 1
- Aluminum complexes 1
- Aluminum indium complex ring opening polymn catalyst kinetics polylactide 1
- Alzheimer 1
- Amide 1
- Amides 1
- Amidinate ligands 1
- Amidine 1
- Amido complexes 1
- Amination 1
- Amines 2
- Amino acids 2
- Amino-acids 1
- Amino alcohols 1
- Aminoboranes 2
- Aminoboronic 1
- Aminochalcones 1
- Aminocyclopentitols 1
- Amino ketones 1
- Amino-ynone 1
- Ammonium 1
- Ammonium bifluoride 1
- Amorphous 1
- Amorphous materials 1
- Amorphous powders 1
- Analogues 1
- Analytical Chemistry 1
- Aniline 2
- Anilines 1
- Anions 1
- Annulation 1
- Anodes 1
- Anodic cyanation 1
- Antenna Effect 1
- Antennas 1
- Anti-apoptotic proteins 1
- Antibacterial activity 2
- Antibacterial activity and thermal analysis TG/DTA 1
- Antibacterial and anti-fungal activities 1
- Antibacterial study 1
- Anticancer activity 1
- Anticancer agents 1
- Anti-counterfeiting 1
- Antiferromagnetism 1
- Antifungal activity 2
- Antifungal and antioxidant activities 1
- Antifungal and biological activities 1
- Antimalarial activity 1
- Antimicrobial activity 4
- Antimicrobial evaluation 1
- Antimony 1
- Antioxidant activity 6
- Antioxidant and antifungal activities 1
- Antioxidant and antifungal properties 1
- Antioxidant properties 1
- Antiparasitic agents 1
- Antiproliferative activity 6
- Antireflection coatings 1
- Anti reflective coatings 1
- A optical materials 1
- A Optical materials 1
- Applied magnetic fields 1
- A Rare-earth intermetallics 1
- Aromatic compound 1
- Aromatic compounds 1
- Arsenide 1
- Article 1
- Artificial photosynthesis 1
- Aryl 1
- Arylation 2
- Aryl bromides 2
- Arylchalcogenoborate 1
- Arylimines 1
- As–Sb–Se glass 1
- Assemblage de protéine 1
- Assignment 1
- Association rates 1
- Asymmetric catalysis 2
- Asymmetric cyanosilylation 1
- Asymmetric hydrophosphination 1
- Asymmetric siloxanes 1
- Asymmetric synthesis 4
- Atmospheric temperature 1
- Atomic force microscopy 1
- Atomic level structure 1
- Atom transfer radical polymerization 1
- Atropisomers 2
- Augmented-wave method 1
- Aurocycle 1
- Aurocycles 1
- Axial anisotropy 1
- Axial chirality 2
- Azafluorenone 1
- Azanalogues 1
- Aza-Prins 1
- Aza-β3-pseudopeptides 1
- Azepines 1
- Azide 1
- Azole 1
- Azoles 1
- Azoxybenzene-3 3’ 5 5’-tetracarboxylic acid 1
- B8-type substructure 1
- Band gap 2
- Band-selective 1
- Band structure 1
- Barium 9
- Barium compounds 1
- Barrier properties 1
- Base-mediated halogen dance 1
- BaSnO3 1
- B Crystal chemistry of intermetallics 1
- B crystal growth 1
- B Electrical resistance and other electrical properties 1
- Benzaldehydes 1
- Benzenesulfonamide Schiff base CuII–complexes 1
- Benzenesulfonyl chlorides 1
- Benzimidazole 1
- Benzimidazole-2-thione 1
- Benzimidazoles 1
- Benzimidazolium salts 1
- Benzo12-b 45-b' dithiophene-48-dione C-H bond functionalization DFT calculations homogeneous catalysis photophysical properties 1
- Benzodiazepine 1
- Benzofuran 2
- Benzofuran benzothiophene bimetallic base polycyclic compound copper 1
- Benzofurans 1
- Benzothiophene 2
- Benzoxaborole 1
- Beta-diketonate 1
- Beta-diketone 1
- Beta-Lactams 1
- Beta-lactoglobulin 1
- Beta-lactoglobuline 1
- Betti bases 1
- BF 1
- Biaryl arylazine prepn deprotonation regioselectivity Gibbs energy 1
- Bicyclic products 1
- Bicyclo222 backbone 1
- Bifunctional chelates 1
- Bimetallic 1
- Bimetallic base 1
- Bimetallic bases 1
- Bimetallic complex 2
- Bimetallic complexes 2
- Bimetallic exsolution 1
- Bimetallic strip 1
- Binaphtyl 1
- Binding modes 1
- Binol 1
- BINOL 3
- Binuclear complex 1
- Binuclear zinc complexes 1
- Bioactive glass 1
- Bioactive Glass 1
- Bioactive glasses 1
- Bioactive molecules 1
- Bioactivity 1
- Bioassays 1
- Biocompatible NPs 1
- Biological activities 1
- Biological activity 3
- Biological evaluation 1
- Biological study 2
- Bipyrimidine 1
- Bis-heterocycles 1
- Bismuth 3
- Bism-xylylenediaminium hexachlorocadmateII 1
- Bis-phenols 1
- Bisphosphate 1
- Bisphosphonate 1
- Bispyrazole 1
- Bispyridone 1
- Bispyrone 1
- BIS-TETRATHIAFULVALENES 1
- Bisσborate 1
- B luminescence 1
- B lymphocyte cell 1
- B Magnetic properties 2
- BN compounds 1
- BODIPY 2
- Bond formation 1
- Bonding analysis 1
- Bonding interactions 1
- Bond-valence sum 1
- B optical properties 1
- Borane 2
- Boranes 2
- Boranil 2
- Borasiloxane 2
- Borate 3
- Borates 2
- Boride 1
- Borohydride complexes 1
- Boron 10
- Boron difluoride 1
- Boron difluoride complex 1
- Boronic 1
- Borophosphate fiber 1
- Borophosphate glasses 1
- Borosilicate glasses 1
- Borylene 2
- Boryloxide 1
- Bridge-centered radicals 1
- Brønsted Acid 1
- Bulky bipyridine ligands 1
- Bulky siloxide 1
- C3H74P2Cd2Br6 1
- C-60 1
- C9H15N3CdCl4 complex 1
- Ca2+ signalling 1
- Cadmium 4
- Cadmium geometry 1
- CadmiumII porphyrin complex 1
- CadmiumII porphyrin coordination compound 1
- Cadmium overhanging carboxylic acid porphyrin complex prepn crystal structure 1
- Cadmium porphyrin 1
- Cadmium porphyrin complex 1
- Caking 1
- Calcium 4
- Calcium-fluorine interactions 1
- Calculations 1
- Cancer 2
- Carbamate 1
- Carbamate derivatives 1
- Carbazolate 1
- Carbazolate ligand 1
- Carbene 1
- Carbenes 2
- Carbohydrates 2
- Carbon 1
- Carbon bond formation 1
- Carbon dioxide 1
- Carbon-dioxide 1
- Carbon dioxide fixation 1
- Carbon disulfide 1
- Carbonyl complex 1
- Carbonyl complexes 1
- Carbonyl-complexes 1
- Carbonyl ligands 1
- Carbonyl ylides 1
- Carboxamide 3
- Carboxylic Acids/chemistry 1
- Carboxylic esters 1
- Cascade 1
- Cascade process 1
- Cascade reactions 1
- Catalysis 12
- Catalysis C-C bond formation 1
- Catalyst 3
- Catalyst loadings 1
- Catalyst selectivity 1
- Catalytic activity 2
- Catalytic degradation of the rhodamine B dye DFT calculations 1
- Catalytic hydrophosphonylation 1
- Catalytic oligomerization 1
- Catalytic performance 1
- Catalytic reactions 1
- Catalyzed C-C coupling 1
- Catalyzed intermolecular hydrophosphination 1
- Catecholase activity and CopperII complex 1
- Catechol oxidase 1
- Catechol oxidation 1
- Cation 1
- Cation binding 2
- Cationic complexes 1
- Cationizing agents 1
- Cation radicals 1
- Cations 1
- C bond formation 1
- C-c bond formation 1
- C-C bond formation 1
- C-C coupling 1
- CdII complex 1
- Cells attachment 1
- Center-dot-licl 1
- CePt5Sb 1
- Ceramics 2
- Cerium platinum antimonide 1
- Cesium alloys 1
- CH acidity 3
- CH-acidity 1
- Ch acidity relationships 1
- C-H acti- vation 1
- C-H activation 1
- C–H activation 2
- C−H activation 1
- CHAIN-TRANSFER 1
- Chalcogen 2
- Chalcogen-bridged 1
- Chalcogenide glass 5
- Chalcogenide glasses 3
- Chalcogenides 1
- Chalcogenolato-bridge 1
- Chalcogens 2
- Chalcohalide glass 1
- Chalcones 1
- Characterization 2
- Characterization materials science 2
- Characterization of inorganic materials 1
- Charge container 1
- Charge localization 1
- Charge Transfer 1
- CHARGE-TRANSFER 1
- Charge transfer salt 1
- Charge transport 1
- C-H bond activation 1
- C–H bond activation 1
- CH-bond activation 1
- C-H bond cleavage 1
- C–H bond deprotonation 1
- C-H bond functionalization 4
- C-H borylation 1
- CH⋯Br interactions 1
- Chelate ligand 1
- Chelates 1
- Chelating ligand 1
- Chelating ligands 1
- Chelation 1
- Chemical docking 1
- Chemical formula 1
- Chemical mechanism 1
- Chemical physics 1
- Chemical preparation 1
- Chemical reactions 2
- Chemical reactivity 1
- Chemical reactivity DFT 1
- Chemical structure 3
- Chemical synthesis 4
- Chemistry 8
- Chemistry/Food Science 1
- Chemometry 1
- Chevrel phases 1
- C−H functionalization 1
- Chiral amine 1
- Chiral ancillary ligand 1
- Chiral auxiliaries 2
- Chiral base 1
- Chiral bisoxazoline synthesis 1
- Chiral cyclic imine 1
- Chiral directing group 1
- Chiral dopant 1
- Chiral goldIII homodimeric complexes 1
- Chiral halogenometallate 1
- Chiral hybrid halide 1
- Chirality 12
- Chiral nitrogen atom 1
- Chiral phosphates 1
- Chiral phosphotriesters 2
- Chiral polymers 1
- Chiral porphyrins 1
- Chiral properties 1
- Chiral resolution 2
- Chiral solvating agents 1
- Chiral symmetry breaking 1
- Chiral β-diketones 1
- Chiral β-Diketones 1
- Chiroptical activity 1
- Chiroptical properties 3
- Chiroptics 1
- Chitosan 1
- Chloride ion 1
- Chlorine compounds 1
- Chlorobismuthate 1
- Chlorocadmate 1
- Chromaborane 1
- Chromane 1
- Chromanequinoline 1
- ChromateVI 1
- Chromone 1
- CH⋯π interactions 1
- Circular dichroism 3
- Circular Dichroism 1
- Circular dichroisme 1
- Circularly polarized emission 2
- Circularly polarized luminescence 6
- Circularly Polarized Luminescence 1
- Circular polarization 1
- Circumsporozoite protein of Plasmodium berghei 1
- Claisen-Schmidt reaction 1
- Classical mechanics 1
- Clathrates 1
- Cleavage studies 1
- Cluster 2
- Cluster-based hybrid nanomaterials 1
- Cluster chemistry 1
- Cluster compound 1
- Cluster compounds 8
- Cluster- or spin-glass behavior 1
- Clusters compounds 1
- C-N bond formation 1
- Co2 reduction 1
- Coacervation 1
- Coatings 1
- Cobalt 4
- Cobalt complexes 1
- CobaltII 2
- CobaltII-porphyrin framework 1
- CobaltII porphyrins 1
- Cobalt mixed valance complexes 1
- Co−Fe alloy nanoparticles 1
- Color 1
- Column chromatography 1
- Combinatorial chemistry 1
- Combustion synthesis 1
- Complete crystallization 1
- Complex 1
- Complexation 1
- Complex compound 1
- Complexes 3
- COMPLEXES 3
- Complexes/chemistry 1
- Compleximpedance 1
- Composite 1
- Compounds u3m2m'3 1
- Computational chemistry 2
- Computational investigation 1
- Computational studies 1
- Computer science 1
- Condensation 1
- Condensation reactions 1
- Condensed matter physics 1
- Conducting materials 1
- Conduction mechanism 4
- Conductivity 1
- Conformation 1
- Conformation analysis 1
- Continuous flow 1
- Cooperative effects 1
- Coordinated olefin 1
- Coordination 4
- Coordination chemistry 2
- Coordination Complexes/chemistry 1
- Coordination compounds 1
- Coordination modes 3
- Coordination polymers 1
- Coordination Polymers 1
- Coordination polymers Porosity Crystal structure Lanthanide Green Chemistry 1
- Coordination sphere 1
- Copolymers 1
- Copolymers end-functionalized with peptide 1
- Copper 18
- Copper catalysis 1
- Copper complex 1
- Copper complexes 1
- Copper coordination polymers 1
- CopperII 2
- CopperII complex 1
- Corrosion 1
- Coumarin derivative 1
- Coupled substitution 1
- Coupling 2
- Coupling reaction aryl hetaryl iodide prepn polycyclic arom heterocycle 1
- Coupling reactions 2
- Covalent bond 1
- COVID-19 2
- CPL 2
- CPMG 1
- Crack healing 1
- Crankshaft-type 1
- Cristallisation 1
- Cross-coupling 5
- Cross coupling reactions 1
- Cross-dehydrocoupling 1
- Crossed-aldol 1
- Crucial parameters 1
- Crystal atomic structure 1
- Crystal engineering 1
- Crystal field 1
- Crystal-field splitting 1
- Crystalline structure 1
- Crystallography 8
- Crystal programming language 1
- Crystal structure 61
- Crystal-structure 2
- Crystalstructure 1
- CRYSTAL-STRUCTURE 2
- Crystal structure analysis 1
- Crystal structure dimetallaborane Group 6 element chalcogen cluster erratum 1
- Crystal structure fluorinated alkoxyimino aluminum prepn catalyst polymn lactone 1
- Crystal structure lead isopropoxide amide complex 1
- Crystal structureLuminescent properties 1
- Crystal structure mol iron pentamethylcyclopentadienyl dicarbonyl complex prepn 1
- Crystal-structure refinement 1
- Crystal structures 1
- Crystal-structures 2
- Crystal structure titanocene complex thiazolinethione dithiolate diselenolate ligand 1
- CsbndH bond functionalization 1
- Ct-DNA binding 1
- Ct–DNA binding 1
- Ct-DNA binding studies 1
- CuII complex 1
- CuII complexes 1
- CuII one-dimensional coordination polymer 1
- Curie temperature 1
- CuxMo6S8 1
- C X-ray diffraction 1
- Cyanate 1
- Cyanide 1
- Cyanides 2
- Cyclicalkylaminocarbene 1
- Cyclic esters 1
- Cyclic imine 1
- Cyclic terpenes 1
- Cyclic thioureas 1
- Cyclic urea 1
- Cyclic Voltametry of rutheniumII 1
- Cyclic voltammetry 13
- Cyclic Voltammetry 1
- Cyclisation 2
- Cyclization 2
- Cycloaddition 4
- Cycloalkanones 1
- Cyclobenzaprine 1
- Cyclohydroamination 1
- Cyclometalation 2
- Cyclometallated 1
- Cyclometallated complexes 1
- Cyclopentadienyls 1
- Cyproheptadine 1
- Cytotoxic activity 1
- Cytotoxicity 1
- DABCO ligand 1
- D Crystal structure 1
- Deacetylation 1
- Deactivation 1
- DECOMPOSITION 1
- Decomposition pathway 1
- Deconvolution screening 1
- Degradation of 4-nitrophenol 1
- Dehydroacetic acid 3
- Dehydroacetic acid derivative 1
- Dehydrocoupling catalysis 3
- Dehydrogenative coupling 1
- D Electrical properties 1
- D electronic structure 1
- DELTA-E-1/2 VALUES 1
- Density functional calculation 1
- Density functional calculations 10
- Density functional theory 1
- Density-functional theory 2
- Density Functional Theory 1
- Density function calculations 1
- Dependence chemoselectivity iron mediated metalation substrate electrophile 1
- Deprotolithiation 1
- Deproto-metalation 1
- Deprotometalation 6
- Deprotometallation 2
- Deprotonation 1
- Deprotonative metalation 5
- Derivatives 3
- DESIGN 1
- Desilylation 1
- Desulfinylation 1
- DFT 18
- DFT and ab initio 1
- Dft and tddft calculations 1
- DFT and TD-DFT calculations 2
- DFT and TDDFT calculations 2
- DFT approach 1
- DFT calculation 2
- DFT calculations 20
- DFT-calculations 1
- DFT Calculations 1
- DFT computations 1
- DFT reactivity indices 1
- DFT studies 2
- DFT study 1
- Dialkyl gallium complex 1
- Diamine 1
- Diaminocarbenes 1
- Diaminonaphthalene 1
- Diastereoselective deprotolithiation 1
- Diastereoselectivity 1
- Diasteromerization 1
- Diazepine 1
- Diazines 1
- Diazoacetacetylferrocene 1
- Diazoalkanes 1
- Diazo ester 1
- Di-charged imidazolium ligand 1
- Dichloromethane 1
- Dichroism 1
- Dielectric conductivity 1
- Dielectric properties 1
- Dielectric property 1
- Diels-Alder catalysis 1
- Dienes 1
- Diffraction des rayons X 1
- Digallane complex 1
- Digital storage 1
- Dihedral angle 1
- Dihydropyrone 1
- Diiron nonacarbonyl 1
- Diketonate complex 1
- Diketopyrrolopyrrole 1
- Dimerization 2
- Dimetallaborane cluster Group 6 prepn structure optimized geometry erratum 1
- Dinuclear 1
- Dinuclear complex 2
- Dinuclear complexes 1
- Dioxygen reduction 1
- Dipicolinic acid 1
- Dipole transition moment 1
- Diprotonated porphyrin 1
- Dipyrazolylpyridine 2
- Dipyridylamine 1
- Dipyrrins 1
- Dipyrromethanes 1
- Diradical 1
- Direct arylation 2
- Direct c-2 arylation 1
- Directed lithiation 1
- Di-schiff base 1
- Diselenolene 1
- Disordered crystal structure 1
- Disubstitution 1
- Disulfides 1
- DITHIADIAZAFULVALENES 1
- Dithiafulvalene 1
- Dithioacetate 1
- Dithiol 1
- Dithiolene 3
- DITHIOLENE 1
- Dithiolene ligand 1
- Dithiolene ligands 1
- Divalent cation 1
- D Magnetic properties 1
- Dn/dT 1
- Docking calculation 1
- Domino reactions 1
- Donor-acceptor systems 1
- Doped germanium 1
- Doped TiS2 1
- D Optical properties 1
- Double-chains 1
- Double exchange 1
- DPPH 1
- Drug-RNA interaction 1
- Drug synthesis 1
- Dry reforming of methane 2
- DSC 3
- Dual emission 1
- Dynamics 1
- Dysprosium 13
- Dysprosium compounds 2
- Earth abundant transition metals 1
- Earth metal-complexes 1
- Edible films 1
- Effective concentration 1
- EFFECTIVE CORE POTENTIALS 2
- Efficient dimerization 1
- Efficient hydrosilylation 1
- Elastic moduli 1
- Electrical conductance and dielectric properties 1
- Electrical conductivity 1
- Electrical esistivity 1
- Electrical properties 4
- Electrical transport 3
- Electric properties 2
- Electroactive ligands 1
- Electro-activity 1
- Electrocatalysis 1
- Electrocatalytic reduction 1
- Electrochem 1
- Electrochem and redox modulation of magnetic relaxation of dinuclear dysprosium thenoyltrifluoroacetonate complex with ruthenium acetylide ligand SMM 1
- ELECTROCHEMICAL-BEHAVIOR 1
- Electrochemical electrodes 1
- Electrochemical impedance spectroscopy 1
- Electrochemical performance 1
- Electrochemical properties 1
- Electrochemistry 5
- Electrode material 1
- Electrodeposition 1
- Electrodes 1
- Electromagnetism 1
- Electron acceptor 1
- Electron and synchrotron X-ray diffraction 1
- Electron-donating group 1
- Electronic circular dichroism 1
- Electronic conduction 1
- Electronic coupling 2
- Electronic effect 1
- Electronic interaction 1
- Electronic properties 2
- Electronic structure 1
- Electron microprobe analysis 1
- Electron microscopy 2
- Electron withdrawing group 1
- Electrophilicity 1
- Electropolymerization 1
- Electrospray mass spectrometry 1
- Electrostatic interactions 1
- ELF 2
- Embedded systems 1
- Enamines 2
- Enaminone 1
- Enantiomer 1
- Enantiomeric resolution 1
- Enantiomorphic crystal 1
- Enantiopure 1
- Enantioselective hydrosilylation 1
- Enantioselective synthesis 1
- Enantioselectivity 3
- Energy 1
- Energy conversion 3
- Energy dispersive X ray analysis 1
- Enol ethers 1
- Enone 1
- Enones 1
- Enrichment ratio 1
- Entropy 1
- Enynes 1
- Epitaxy 1
- EPR spectroscopy 1
- Epsilon-caprolactone 1
- Epsilon-caprolactone polymerization 1
- Erratum metallaborane cluster Group 6 prepn structure optimized geometry 1
- Ester 1
- Ester hydrogenation 1
- Esters 1
- EtBr displacement 1
- Ether 1
- Etherification of aldehydes 1
- Ethyl Carbamate 1
- Ethylene 2
- ETHYLENE 1
- Ethylenediamine 1
- Ethylene Diamine 1
- Europium 1
- Evaporation 1
- EXCITATION 1
- Excited state 1
- Excited states 1
- Exciton coupling 1
- Expansion 1
- Extended Framework 1
- Extended-tetrathiafulvalene 1
- Facial 1
- Fe 3 O 4 1
- Fe complex 1
- Feii complexes 1
- FeIII complex 1
- Ferrate complex 1
- Ferrites 1
- Ferrocene 20
- Ferrocene-containing enaminone 1
- Ferrocenes 1
- Ferrocenyl 1
- Ferrocenyl-derivatives 1
- Ferroelectric properties 1
- Ferromagnetic coupling 1
- Ferromagnetism 1
- Ferrous Compounds/chemistry 1
- Fingerprint maps 1
- Five-membered aromatic heterocycles 1
- Flavonoid 1
- Fluorene 2
- Fluorescence 11
- Fluorescence recovery after photobleaching 1
- FLUORESCENCE SWITCH 1
- Fluoride 1
- Fluoride nanocrystals 1
- Fluorinated compounds 1
- Fluorinated NHC 1
- Fluorinated solvent 1
- Fluorine 6
- Fluorine compounds 1
- Fluoroalkoxide 1
- Fluoroarylsilylamides 1
- Fluorosilicate glass 1
- Fogoite-y 1
- Fogo volcano 1
- Foldamers 1
- Force field 1
- Formation mechanism 1
- Formic acid 1
- Four-Component Reaction 1
- Free base porphyrin 1
- Free radical polymerization 1
- Free radicals 1
- Friedländer reaction 1
- Frustrated spin systems 1
- FT-IR 1
- FT-IR and NMR spectroscopies 1
- FT-Raman spectroscopy and NMR 1
- Fukui 1
- Fukui function 1
- Fumaric acid 1
- Functional group manipulation 1
- Functionalization 1
- Functionalized compounds 1
- Fusion 1
- F X-ray diffraction 1
- Ga 1
- Gallium 2
- Gallium group 13 compounds 1
- Gamma lactams 1
- GB virus A 1
- Gem-difluoroalkyl derivatives 1
- Gem-difluoropropargyl 1
- Gem-difluoropropargyls 1
- General 1
- Ge⋯Ni interactions 1
- Germanium 1
- Germylenes 1
- GIANT PORES 1
- Glass 3
- Glass bonding 1
- Glass ceramics 1
- Glass matrix composite 1
- Glass reactivity in SBF 1
- Gold 3
- Gold bisdithiolene complexes 1
- Gold complex 1
- GoldI 1
- GoldIII complexes 1
- Gold nanoparticles 1
- Gotzenite 1
- Graphite felt 1
- Group 4 metallocenes 1
- Group 9 1
- Group i 1
- Growth 1
- GSK3 1
- H activation 1
- Hafnium 1
- HAFNIUM 1
- Hainite 1
- Half integer quadrupolar nucleus 1
- Half-quantities 1
- Halides 1
- Halogenation 1
- Halogen bonding 1
- Halogen bonds 1
- Halogen dance 1
- Halogen migration 1
- Halogenometallates 1
- Halogne pnicture 1
- Haloimidazole 1
- H-bonded system 1
- Heat 1
- Heat capacity 1
- Heavier alkaline-earths 1
- Heavy doping 1
- Heavy fermions 1
- Heavy metals 1
- Heck 1
- HELICAL CHAINS 1
- Helicene 11
- Helicenes 5
- Hematite 1
- Heme/chemistry 1
- Hemilabile 1
- Hemolytic activity 1
- HepaRG cells 1
- Hepatotropic peptides 1
- Heteroarenes 2
- Heteroatoms 1
- Heterocycle 3
- Heterocycles 17
- Heterocyclyl methanol regioselective prepn 1
- Heterodinuclear complex 1
- Heteroleptic tin initiator ring opening polymn lactide trimethylene carbonate 1
- Heterometallic 1
- Heteronuclear scalar interaction 1
- Hexachlorobismuthate 1
- Hexafluorophosphate salt 1
- High-performance liquid chromatography 1
- High resolution transmission electron microscopy 1
- High-temperature electrochemical 1
- High-temperature in situ 1
- High throughput experimentation 1
- High throughput screening 1
- HMBC 1
- HOMOand8211 1
- HOMO-LUMO 2
- HOMO/LUMO 1
- HSA interaction 1
- HSQC 1
- HYDROTHERMAL SYNTHESIS 2
- -valerolactone 1
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