Publication | Closed Access
Order−Disorder Transitions in Self-Assembled Monolayers: A <sup>13</sup>C Solid-State NMR Study
81
Citations
21
References
1997
Year
EngineeringMolecular Self-assemblyMagnetic ResonanceSurface NanotechnologyChemistryChain Length DependenceOrder−disorder TransitionsChain LengthMaterials SciencePhysicsPhysical ChemistryLayered MaterialSurface ChemistryNatural SciencesSelf-assemblySurface ScienceCondensed Matter PhysicsApplied PhysicsChain LengthsNuclear Magnetic Resonance Spectroscopy
The effect of the chain length and temperature on ordering of alkylphosphonate, (CnH2n+1)PO3H2, n = 8−18, monolayers on ZrO2 was characterized by solid-state 13C NMR. Alkylphosphonate monolayers with chain lengths of n < 16 are disordered at room temperature. C18 monolayers of thiols and phosphonates both show reversible chain melting at ∼50 °C. This chain length dependence, as well as variable-temperature spectra, demonstrates that the thermal stabilities of conformational order in phosphonate and thiol monolayers are similar. In general, the initial free volume in a self-assembled monolayer on a rough surface is large enough to allow reversible thermal disordering although the headgroup remains rigid.
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