@article {2630,
	title = {A new [4]carceplex, and a crystal structure and dynamic combinatorial chemistry of a [5]carceplex},
	journal = {Tetrahedron},
	volume = {65},
	number = {35},
	year = {2009},
	note = {ISI Document Delivery No.: 485CQTimes Cited: 1Cited Reference Count: 16Sun, Jianyu Patrick, Brian O. Sherman, John C.},
	month = {Aug},
	pages = {7296-7302},
	type = {Article},
	abstract = {A new [4]carceplex (2-guest) is reported. It is composed of two cavitands linked by four disulfide bonds. It forms twistomers, which interconvert on a millisecond timescale. The energy barrier for interconversion of twistomers is guest-dependent. Formation of [4]carceplex 2-guest is template dependent. The selectivity in templates is flat relative to most previous related template work. Larger kin [5]carceplex 1.guests were reinvestigated. A crystal structure confirms the twist between the hemispherical cavitands. Use of a redox buffer allowed dynamic combinatorial chemistry to be performed between pairs of templates. (C) 2009 Elsevier Ltd. All rights reserved.},
	keywords = {carceplex, Disulfide, Dynamic combinatorial chemistry, Guest release, HEMICARCEPLEXES, MOLECULES, supramolecular, TEMPLATION},
	isbn = {0040-4020},
	url = {<Go to ISI>://000269098700012},
	author = {Sun, J. Y. and Patrick, B. O. and Sherman, J. C.}
}
@article {2332,
	title = {Facile Synthesis of Unsubstituted beta,beta {\textquoteright}-Linked Diformyldipyrromethanes},
	journal = {Journal of Organic Chemistry},
	volume = {73},
	number = {23},
	year = {2008},
	note = {ISI Document Delivery No.: 378JDTimes Cited: 2Cited Reference Count: 31Zhang, Zhan Shin, Ji-Young Dolphin, David},
	month = {Dec},
	pages = {9515-9517},
	type = {Article},
	abstract = {Unsubstituted beta,beta{\textquoteright}-linked diformyldipyrromethanes are promising precursors for the synthesis of novel poly dipyrromethene ligands and N-confused porphyrins. A strategy has been developed to selectively synthesize unsubstituted beta,beta{\textquoteright}-linked diformyldipyrromethanes in moderate yields starting from 2-formylpyrrole.},
	keywords = {ACETALS, BUILDING-BLOCKS, CHEMISTRY, COMPLEXES, ISOMER, MESOSUBSTITUTED DIPYRROMETHANES, N-confused porphyrin, SALTS, SUBSTITUENTS, supramolecular, TETRAPYRROLE},
	isbn = {0022-3263},
	url = {<Go to ISI>://000261316100052},
	author = {Zhang, Z. and Shin, J. Y. 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 {1116,
	title = {Synthesis, structure, and computational studies of soluble conjugated multidentate macrocycles},
	journal = {J. Org. Chem.},
	volume = {70},
	number = {20},
	year = {2005},
	note = {ISI Document Delivery No.: 968MOTimes Cited: 47Cited Reference Count: 67},
	month = {Sep},
	pages = {7936-7946},
	type = {Article},
	abstract = {<p>Conjugated, shape-persistent macrocycles based on [3 + 3] Schiff-base condensation are of interest for supramolecular materials. In an effort to develop new discotic liquid crystals based on these compounds, a series of macrocycles with peripheral alkoxy groups of varying length have been prepared. The synthesis and mechanism of formation have been probed by isolation of oligomeric intermediates. A single-crystal X-ray diffraction study of one macrocycle revealed a nonplanar, strongly hydrogen-bonded structure. To our surprise, even with very long substituents, the macrocycles were not liquid crystalline. This has been rationalized by ab initio calculations that indicate the macrocycles are undergoing rotation of the dibydroxydiiminobenzene rings that may not allow a stable discotic liquid crystalline phase. These results provide new insight into the formation and properties of these large macrocycles and may provide guidance to developing stable liquid crystalline materials in the future.</p>},
	keywords = {CHEMISTRY, CRYSTAL-STRUCTURE, cyclodextrin, LIGANDS, LIQUID-CRYSTAL, METAL-COMPLEXES, porphyrins, RECEPTORS, SCHIFF-BASE MACROCYCLES, SHAPE-PERSISTENT MACROCYCLES, supramolecular},
	isbn = {0022-3263},
	url = {<Go to ISI>://000232166800015},
	author = {Gallant, A. J. and J. K.-H. Hui and Zahariev, F. E. and Y. A. Wang* and M. J. MacLachlan*}
}
@article {678,
	title = {Template effect where 1-3 molecules drive formation of a trimer carceplex},
	journal = {Chemistry-a European Journal},
	volume = {9},
	number = {14},
	year = {2003},
	note = {ISI Document Delivery No.: 706XATimes Cited: 6Cited Reference Count: 46},
	month = {Jul},
	pages = {3253-3262},
	type = {Article},
	abstract = {The template effect in the formation of a trimer carceplex using 1-3 molecules as templates is explored. Thirteen different templates were studied and template ratios were measured for templates of like and unlike molecularity. Five transition-state models were studied for their binding abilities to see if these mirror the template ratios. The chemical shifts of the guests and the thermodynamic and kinetic values for templation suggest that binding is key, often tight, and that the guest determining step is formation of the last covalent bond. The molecular dynamics of guests as well as the conformational dynamics of both hosts and guests further addresses nature of the recognition between host and guest. Finally, we were surprised to discover that water can bind reversibly to the trimer carceplexes, which will have ramifications to any inner phase reactions conducted inside the cage.},
	keywords = {AMPLIFICATION, BARRIER, BINDING, CAPTURE, carceplex, CHEMISTRY, DIELS-ALDER REACTION, DYNAMICS, ELUCIDATION, ENCAPSULATION, HOST-GUEST COMPLEXATION, host-guest systems, molecular recognition, RESORCINARENE CAPSULE, REVERSIBLE, supramolecular, TEMPLATE SYNTHESIS},
	isbn = {0947-6539},
	url = {<Go to ISI>://000184479300009},
	author = {Makeiff, D. A. and Sherman, J. C.}
}
@article {5154,
	title = {Expanding cavitand chemistry: The preparation and characterization of [n]cavitands with n >= 4},
	journal = {Chemistry-a European Journal},
	volume = {7},
	number = {8},
	year = {2001},
	note = {ISI Document Delivery No.: 426VFTimes Cited: 21Cited Reference Count: 26},
	month = {Apr},
	pages = {1637-1645},
	type = {Article},
	abstract = {{The preparation of cavitands composed of 4, 5, 6, and 7 aromatic subunits ([n]cavitands},
	keywords = {CAVITANDS, chemical exchange, CHEMICAL-EXCHANGE, CHEMISTRY, HOST GUEST COMPLEXATION, host-guest chemistry, KINETICS, NMR, supramolecular},
	isbn = {0947-6539},
	url = {<Go to ISI>://000168368500009},
	author = {Naumann, C. and Roman, E. and Peinador, C. and Ren, T. and Patrick, B. O. and Kaifer, A. E. and Sherman, J. C.}
}
@article {3520,
	title = {CARCEPLEXES AND HEMICARCEPLEXES - MOLECULAR ENCAPSULATION - FROM HOURS TO FOREVER},
	journal = {Tetrahedron},
	volume = {51},
	number = {12},
	year = {1995},
	note = {ISI Document Delivery No.: QN982Times Cited: 70Cited Reference Count: 124},
	month = {Mar},
	pages = {3395-3422},
	type = {Review},
	keywords = {4, CARBON NANOTUBES, CARCERANDS, CAVITANDS, CHEMISTRY, CONSTRICTIVE BINDING, CONTAINER COMPOUNDS, HEMICARCERANDS, HOST-GUEST COMPLEXATION, PORTALS, SHELL CLOSURE, supramolecular},
	isbn = {0040-4020},
	url = {<Go to ISI>://A1995QN98200001},
	author = {Sherman, J. C.}
}
