@article { ISI:000187972500016,
	title = {Anthracene-functionalized polystyrene random copolymers: Effects of side-chain modification on polymer structure and behavior},
	journal = {Macromolecules},
	volume = {37},
	number = {1},
	year = {2004},
	month = {JAN 13},
	pages = {92-98},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {Copolymers consisting of styrene and 4-chloromethylstyrene (CMS) were functionalized via reaction with 9-anthracenecarboxylic acid, providing the corresponding esters. Increasing degrees of functionalization were found to increase the glass transition temperature, influence chain packing density, and induce microphase separation in block copolymer structures. The approach demonstrated in this study facilitates the investigation of the relationship between structure of side-chain groups and polymer properties, providing a general approach for the study of the effect of chemical functionality on material properties of polymers.},
	issn = {0024-9297},
	doi = {10.1021/ma035488d},
	author = {Shenhar, R and Sanyal, A and Uzun, O and Rotello, VM}
}
@article { ISI:000220663800005,
	title = {Calculations of PAH anions: When are diffuse functions necessary?},
	journal = {Physical Chemistry Chemical Physics},
	volume = {6},
	number = {6},
	year = {2004},
	month = {MAR 21},
	pages = {1113-1121},
	publisher = {ROYAL SOC CHEMISTRY},
	type = {Article},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {The effect of including vs. excluding diffuse functions while calculating numerous parameters of PAH anions by various calculation methods is discussed. The omission of diffuse functions. appears to have a negligible effect while calculating geometry parameters or total energy; thus, acceptable results may be obtained without them. The conclusions for charge density appear to be the same; however, limited results make an unambiguous claim unachievable. Calculating H-1- and C-13-NMR shifts undoubtedly requires the use of these functions.},
	issn = {1463-9076},
	doi = {10.1039/b315069k},
	author = {Treitel, N and Shenhar, R and Aprahamian, I and Sheradsky, T and Rabinovitz, M}
}
@article { ISI:000222258600026,
	title = {Integration of recognition elements with macromolecular scaffolds: Effects on polymer self-assembly in the solid state},
	journal = {Macromolecules},
	volume = {37},
	number = {13},
	year = {2004},
	month = {JUN 29},
	pages = {4931-4939},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {Polystyrene scaffolds were grafted with model functionalities featuring strongly interacting hydrogen bonding and aromatic stacking elements. Both glass transition temperatures and degree of microphase separation in functionalized block copolymers depend on the nature of the functionality and in particular on the strength of intermolecular interactions. The polymers under study were amorphous; it was found, however, that domain periodicities of functionalized diblock copolymers in the microphase-separated state are extremely sensitive to local interactions between functionalities and can express even subtle differences in interaction strength. The results emphasize the ability to fine-tune polymer microstructure and thermomechanical behavior using supramolecular chemistry.},
	issn = {0024-9297},
	doi = {10.1021/ma0495590},
	author = {Shenhar, R and Sanyal, A and Uzun, O and Nakade, H and Rotello, VM}
}
