Indexed keywords
CHEMICAL REACTIONS;
COMPLEXATION;
COORDINATION REACTIONS;
EXTRACTION;
IONS;
LIGANDS;
METAL IONS;
METAL RECOVERY;
NUCLEAR MAGNETIC RESONANCE;
OXYGEN;
SILVER COMPOUNDS;
SULFUR;
SYNTHESIS (CHEMICAL);
TITRATION;
TRANSITION METALS;
VOLUMETRIC ANALYSIS;
ADAMANTANE;
CHEMICAL EQUATIONS;
COMPLEXING;
COMPLEXING ABILITIES;
CONFORMATIONAL PROPERTIES;
FLEXIBLE CHAINS;
MACROCYCLES;
MACROCYCLIC;
METAL CATIONS;
METHYLENE GROUPS;
NMR TITRATIONS;
OPTIMAL GEOMETRIES;
POLYCYCLIC MOLECULES;
SILVER COMPLEXES;
SOLID STATES;
STERICAL EFFECTS;
STRUCTURE ANALYSIS;
TETRAHEDRAL COORDINATIONS;
TRIFLUOROACETATE;
X-RAY STRUCTURE ANALYSIS;
STRUCTURAL METALS;
3,6,10,13 TETRATHIA 1,8(1,3) DIADAMANTANACYCLOTETRADECAPHANE 2,7,9,14 TETRAONE;
3,6,10,13,17,20 HEXATHIA 1,8,15(1,3) TRIADAMANTANACYCLOHENICOSAPHANE 2,7,9,14,16,21 HEXAONE;
3,6,9,12, TETRATHIA 1(1,3) ADAMANTANACYCLOTRIDECAPHANE 2,13 DIONE;
3,6,9,12,15 PENTATHIA 1(1,3) ADAMANTANACYCLOHEXADECAPHANE 2,16 DIONE;
3,6,9,13,16,19 HEXATHIA 1,11(1,3) DIADAMANTANACYCLOICOSAPHANE 2,10,12,20 TETRAONE;
3,6,9,13,16,19,23,26,29 NONATHIA 1,11,21(1,3) TRIADAMANTANAYCLOTRIACONTAPHANE 2,10,12,20,22,30 HEXAONE;
ADAMANTANE DERIVATIVE;
CARBENE;
CATION;
IONOPHORE;
LACTONE DERIVATIVE;
LIGAND;
MACROCYCLIC COMPOUND;
METAL ION;
OXYGEN;
POLYCYCLIC HYDROCARBON;
SILVER;
SULFUR;
TRANSITION ELEMENT;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL INTERACTION;
CHEMICAL STRUCTURE;
CONFORMATION;
GEOMETRY;
ION PAIR EXTRACTION;
METAL BINDING;
MOLECULE;
NUCLEAR MAGNETIC RESONANCE;
RIGIDITY;
SOLID STATE;
SOLVENT EXTRACTION;
STRUCTURE ANALYSIS;
TITRIMETRY;
X RAY ANALYSIS;
2
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In the reactions of stannapolythianes 3 and 4 with dichloride 21, besides 9 and 11, traces of dimers 10 and 12 were obtained, respectively. Detailed study cf the influence of rigid spacer on macrocyclization, supported by computational analysis, is under investigation
In the reactions of stannapolythianes 3 and 4 with dichloride 21, besides 9 and 11, traces of dimers 10 and 12 were obtained, respectively. Detailed study cf the influence of rigid spacer on macrocyclization, supported by computational analysis, is under investigation.
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