Phenylboronic acids in crystal engineering: Utility of the energetically unfavorable syn,syn-conformation in co-crystal design

Science China Chemistry

Volumn 54, Issue 12, 2011, Pages 1909-1919

  Varughese, Sunil ^a   Sinha, Shashi Bhushan ^a   Desiraju, Gautam R ^a  

^a INDIAN INSTITUTE OF SCIENCE   (India)

Author keywords

conformational flexibility; crystal engineering; phenylboronic acid; supramolecular synthon

Indexed keywords

1 ,10-PHENANTHROLINE; ALPRAZOLAM; ANTI CONFORMERS; BENZOTRIAZOLES; BIPYRIDINES; BORONIC ACID; CO-CRYSTAL FORMATION; CO-CRYSTALS; COCRYSTALLIZATION; CONFORMATIONAL FLEXIBILITY; DESIGN STRATEGIES; DIMER FORMATION; ENERGY FACTORS; ENERGY PROFILE; HETEROCYCLES; HYDROGEN BOND ACCEPTORS; INTERACTION ENERGIES; LADDER STRUCTURES; LATTICE ENERGIES; LINEAR CHAIN; MOLECULAR COMPLEXES; N-HETEROCYCLES; NATIVE STATE; NATIVE STRUCTURES; OH GROUP; PHENOLIC GROUPS; PHENYLBORONIC ACIDS; RELATIVE STABILITIES; SELECTIVE FORMATION; SUPRAMOLECULAR SYNTHONS; SYNTHONS; TETRAZOLES; THEORETICAL CALCULATIONS; THEORETICAL RESULT; WEAK ACIDS; WEAK INTERACTIONS;

CHEMICAL SENSORS; COBALT; COMPLEXATION; CONFORMATIONS; CRYSTAL ENGINEERING; CRYSTALS; DIMERS; FUNCTIONAL GROUPS; HYDROGEN BONDS; MOLECULES; ORGANIC ACIDS; PHENOLS; STRUCTURAL DESIGN;

CRYSTAL ORIENTATION;

EID: 84856224873     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-011-4412-x     Document Type: Article

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