@article { ISI:000480499600068,
	title = {Open Pentiptycene Networks Assembled through Charge-Assisted Hydrogen Bonds},
	journal = {CRYSTAL GROWTH \& DESIGN},
	volume = {19},
	number = {8},
	year = {2019},
	month = {AUG},
	pages = {4829-4835},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {A series of hydrogen-bonded networks was prepared incorporating ditopic, tritopic, or tetratopic polyamidinium tectons and linear pentiptycene dicarboxylates. The ditopic amidinium forms a 1D hydrogen bonded chain when combined with the pentiptycene tecton, while the tritopic trigonal planar amidinium tecton forms a 2D honeycomb network. A tetratopic amidinium tecton forms a 3D diamondoid network, which is 32-fold interpenetrated, tied for the highest degree of interpenetration observed for a hydrogen bonded network. The bulky pentiptycene functionality prohibits the polymers from packing efficiently, leading to voids within each structure. These frameworks were envisaged as potential molecular motors, but unfortunately, a lack of stability to solvent removal precluded an investigation of these properties.},
	issn = {1528-7483},
	doi = {10.1021/acs.cgd.9b00801},
	author = {Boer, Stephanie A. and Wang, Pei-Xi and MacLachlan, Mark J. and White, Nicholas G.}
}
