@article {32775,
	title = {Iron Porphyrins Embedded into a Supramolecular Porous Organic Cage for Electrochemical CO2 Reduction in Water},
	journal = {Angewandte Chemie International Edition},
	volume = {57},
	year = {2018},
	pages = {9684-9688},
	abstract = {<p>Abstract A porous organic cage composed of six iron tetraphenylporphyrins was used as a supramolecular catalyst for electrochemical CO2-to-CO conversion. This strategy enhances active site exposure and substrate diffusion relative to the monomeric catalyst, resulting in CO generation with near-quantitative Faradaic efficiency in pH 7.3 water, with activities reaching 55\&thinsp;250 turnovers. These results provide a starting point for the design of supramolecular catalysts that can exploit the properties of the surrounding matrix yet retain the tunability of the original molecular unit.</p>},
	keywords = {CO2 reduction, ELECTROCHEMISTRY, porous organic cages, porphyrins, supramolecular chemistry},
	doi = {10.1002/anie.201803873},
	url = {https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201803873},
	author = {Smith, Peter T. and Benke, Bahiru Punja and Cao, Zhi and Kim, Younghoon and Nichols, Eva M. and Kim, Kimoon and Chang, Christopher J.}
}
@article {2174,
	title = {Metal complexes of dipyrromethenes linked by rigid spacer arms},
	journal = {Crystengcomm},
	volume = {10},
	number = {11},
	year = {2008},
	note = {ISI Document Delivery No.: 365VFTimes Cited: 3Cited Reference Count: 19Ma, Li Shin, Ji-Young Patrick, Brian O. Dolphin, David},
	pages = {1539-1541},
	type = {Article},
	abstract = {Metal complexes using ligands where two terminal dipyrromethenes are connected by rigid spacers, having different dihedral angles, show unique macrocyclic structures which contain large cavities in their centers and produce crystals with tunnels of varying structures depending upon their crystal packing motifs.},
	keywords = {HELIX, LIGANDS, supramolecular chemistry, TRIMERS},
	isbn = {1466-8033},
	url = {<Go to ISI>://000260436400007},
	author = {Ma, L. and Shin, J. Y. and Patrick, B. O. and Dolphin, D.}
}
@article {2205,
	title = {Template-assembled synthetic G-quartets (TASQs)},
	journal = {Angewandte Chemie-International Edition},
	volume = {47},
	number = {26},
	year = {2008},
	note = {ISI Document Delivery No.: 317SSTimes Cited: 8Cited Reference Count: 38Nikan, Mehran Sherman, John C.},
	pages = {4900-4902},
	type = {Article},
	keywords = {cation, CAVITANDS, CHEMISTRY, DEOXYGUANOSINE, DERIVATIVES, G-quartets, GUANOSINE, HOST-GUEST COMPLEXATION, NUCLEOSIDES, NUCLEOTIDE, ORGANIC-SOLVENTS, QUADRUPLEX STRUCTURE, supramolecular, supramolecular chemistry, SYNTHESIS, TELOMERIC DNA OLIGONUCLEOTIDES, TEMPLATE},
	isbn = {1433-7851},
	url = {<Go to ISI>://000257040800022},
	author = {Nikan, M. and Sherman, J. C.}
}
@article {460,
	title = {Synthesis and characterization of upper and lower rim functionalized [6]cavitands},
	journal = {Chemistry-a European Journal},
	volume = {8},
	number = {16},
	year = {2002},
	note = {ISI Document Delivery No.: 587QETimes Cited: 2Cited Reference Count: 17},
	month = {Aug},
	pages = {3717-3723},
	type = {Article},
	abstract = {A [6]cavitand has been selectively derivatized on both the lower and upper rims. On the lower rim, two out of six potential sites were oxidized to produce a 1,4 substituted [6]cavitand bisketone, which was converted to a corresponding diol as well as a bisacetate [6]cavitand. The crystal structures of the bisketone and the diol were solved. On the upper rim, all six ArCH3 groups were selectively brominated to ArCH2Br groups to produce the hexabromomethyl [6]cavitand, which was converted to the corresponding hexabenzylthiol and hexabenzylthioacetate [6]cavitands. The conformational properties of all compounds are discussed.},
	keywords = {CAVITANDS, CHEMISTRY, interconversion, NMR spectroscopy, supramolecular chemistry},
	isbn = {0947-6539},
	url = {<Go to ISI>://000177652800016},
	author = {Naumann, C. and Patrick, B. O. and Sherman, J.}
}
@article {4577,
	title = {Carceplexes and hemicarceplexes},
	journal = {Chemical Reviews},
	volume = {99},
	number = {4},
	year = {1999},
	note = {ISI Document Delivery No.: 189WZTimes Cited: 258Cited Reference Count: 229},
	month = {Apr},
	pages = {931-967},
	type = {Review},
	keywords = {CONSTRICTIVE BINDING, CRYSTAL-STRUCTURE, DIELS-ALDER REACTION, ENDOHEDRAL METALLOFULLERENES, ENERGY-TRANSFER, HOST-GUEST COMPLEXATION, HYDROGEN-BONDING PREFERENCES, REVERSIBLE MOLECULAR CAPSULES, SELF-ASSEMBLED MONOLAYERS, supramolecular chemistry, TRIPLET},
	isbn = {0009-2665},
	url = {<Go to ISI>://000079930300001},
	author = {Jasat, A. and Sherman, J. C.}
}
@article {3935,
	title = {A bis(carceplex) from a cyclic tetramer of cavitands},
	journal = {Angewandte Chemie-International Edition in English},
	volume = {36},
	number = {16},
	year = {1997},
	note = {ISI Document Delivery No.: XX181Times Cited: 36Cited Reference Count: 35},
	month = {Sep},
	pages = {1727-1729},
	type = {Article},
	keywords = {CALIX<4>ARENE, CARCEPLEXES, CAVITANDS, CHANNELS, CHEMISTRY, COMPLEXES, ENCAPSULATION, HOST, host-guest chemistry, INCLUSION, MOLECULES, self-assembly, supramolecular chemistry, THERMODYNAMICS},
	isbn = {0570-0833},
	url = {<Go to ISI>://A1997XX18100014},
	author = {Chopra, N. and Sherman, J. C.}
}
@article {2864,
	title = {HEXADENTATE N3O3 AMINE PHENOL LIGANDS FOR GROUP-13 METAL-IONS - EVIDENCE FOR INTRASTRAND AND INTERSTRAND HYDROGEN-BONDS IN POLYDENTATE TRIPODAL AMINE PHENOLS},
	journal = {Inorganic Chemistry},
	volume = {32},
	number = {20},
	year = {1993},
	note = {ISI Document Delivery No.: LZ815Times Cited: 37Cited Reference Count: 27},
	month = {Sep},
	pages = {4268-4276},
	type = {Article},
	abstract = {{Several N3O3 amine phenols (H-3L1 = 1,2,3-tris((2-hydrox benzyl)amino)propane; H-3L2 = 1,2,3-tris((5-chloro-2-hydroxybenzyl)amino)propane; H-3L3 = 1,2,3-tris((2-hydroxy-5-methoxybenzyl)amino)propane; H-3L4 = 1,2,3-tris((3,5-dichloro-2-hydroxybenzyl)amino)propane) were prepared and characterized by various spectroscopic methods (IR, FAB-MS, NMR). The N3O3 amine phenols are KBH4 reduction products of the corresponding Schiff bases derived from the condensation reactions of tap (tap = 1,2,3-triaminopropane) with 3 equiv of either salicylaldehyde or ring-substituted salicylaldehydes. Neutral binary metal complexes, [M(L)] (M = Al},
	keywords = {COMPLEXES, COORDINATION CHEMISTRY, MOLECULES, supramolecular chemistry},
	isbn = {0020-1669},
	url = {<Go to ISI>://A1993LZ81500019},
	author = {Liu, S. and Wong, E. and Rettig, S. J. and Orvig, Chris}
}
