Abstract
NMR and STM studies revealed that the hydrazide-quinolinone-based building block 5 exhibited a monomer-dimer-polymer equilibrium, while its acyclic analogue 6, due to conformational flexibility, exhibited a more complicated mode of aggregation and formed a gel in dichloromethane/hexane.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amides / chemical synthesis*
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Amides / chemistry
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Esters / chemical synthesis*
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Esters / chemistry
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Gels / chemical synthesis
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Gels / chemistry
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Hydrogen Bonding
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Magnetic Resonance Spectroscopy / methods
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Microscopy, Scanning Tunneling / methods
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Molecular Structure
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Particle Size
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Quinolones / chemistry*
Substances
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Amides
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Esters
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Gels
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Quinolones