Polyethylenes with halogens placed on each and every 21st, 15th, or ninth backbone carbon display crystallization patterns enabled by the size of the halogen and by changing crystallization kinetics. The different structures have been identified from X-ray patterns combined with a detailed analysis of the infrared spectra of series containing F, Cl, or Br atoms that were either fast or isothermally crystallized from the melt. Under both crystallization modes, all specimens develop layered crystallites that accommodate 5-9 repeating units along the chain's axis.
View Article and Find Full Text PDFA fundamental chemoselectivity challenge that remains intrinsically unsolved in aldol-type reactions is the suppression of self-aldol reactions with enolizable aldehydes in reactions such as cross-aldol processes. Contrasting with the usual practice of using large excesses of one component to compete with the undesired self-aldehyde condensation reactions, we have developed an enzyme-like polymer catalyst consisting of a hyperbranched polyethyleneimine derivative and proline that can eliminate the self-aldol reactions by suppressing an irreversible aldol condensation pathway. Control experiments and preliminary mechanistic studies suggest that the polymer catalyst provides an optimum environment for the aldol reaction to proceed selectively in water, and the catalytic conditions provided by the polymer are difficult to duplicate with typical small molecule analogues.
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