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A C Grimsdale

Publications and source records attributed to A C Grimsdale.

3 recordsLinked to original sources

Characterization of an insoluble poly(9,9-diphenyl-2,7-fluorene) by solvent-free sample preparation for MALDI-TOF mass spectrometry.

The application of solvent-free sample preparation for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) allowed the characterization of an insoluble fraction of poly(9,9-diphenylfluorene) that was previously hindered by the lack of suitable characterization methods. The MALDI mass spectrometric analysis gives valuable mechanistic information about the heterogeneous polymerization process of the insoluble high molecular weight fraction of the polymer. The fragmentation appearing even under moderate desorption and ionization conditions of this rigid backbone analyte is identified as a multiple loss of the bulky phenyl side groups and can be avoided by applying the new MALDI matrix 7,7,8,8-tetracyanoquinodimethane. A specialized fragmentation study by postsource decay MALDI-TOF MS reveals a molecular weight dependent change in fragmentation mechanism from an exclusive cleavage of side groups from long polymer chains to an additional cleavage of the polymer backbone of short polymer chains.

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Polyfluorenes with polyphenylene dendron side chains: toward non-aggregating, light-emitting polymers.

A polyfluorene 12 has been prepared in which bulky polyphenylene dendrimer substituents suppress formation of long wavelength emitting aggregates, thus giving a polymer with pure blue emission. Absorption- and emission spectra and molecular modeling confirm that the bulky dendrimer side chains do not cause extra torsion between the fluorene units. New polyfluorenes with 9,9-diaryl substituents have been prepared to determine the minimum size of substituent necessary for aggregation suppression. An LED using 12 has been demonstrated to produce blue emission with onset voltages below 4 V.

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1- , 2-, and 3-dimensional polyphenylenes--from molecular wires to functionalised nanoparticles.

Polyphenylenes, ranging from one-dimensional wire-like conjugated polymers to two-dimensional disc-shaped polyaromatic hydrocarbons and three-dimensional sphere-like dendrimers, have been prepared using methods that allow synthetic control of their molecular and supramolecular order in order to optimise their physical, especially optical and electrical, properties. 1D-conjugated polymers can be used as emitting materials in LEDs, with their colours tuned so as to give emission across the whole visible spectrum. Their supramolecular order can be manipulated by attachment of bulky sidechains to suppress aggregation, and by formation of rod-coil block copolymers. 2D polycyclic aromatic hydrocarbons form stable columnar mesophases with high charge carrier mobilities. Their size, shape, and substitution patterns can be altered so as to maximise their intra- and intercolumnar order. 3D polyphenylene dendrimers can be prepared in ways that enable control of their shape, and their surfaces can be selectively functionalised in ways that permit them to act as functionalised nanoparticles.

Journal Article↗