@inbook {833,
	title = {Measuring the silion fluoride bond distance in zeolites},
	booktitle = {Recent Advances in the Science and Technology of Zeolites and Related Materials, Pts a - C},
	series = {Studies in Surface Science and Catalysis},
	volume = {154},
	year = {2004},
	note = {ISI Document Delivery No.: BBR47Times Cited: 0Cited Reference Count: 19Proceedings Paper14th International Zeolite Conference on Recent Advances in the Science and Technology of Zeolites and Related MaterialsAPR 25-30, 2004Cape Town, SOUTH AFRICASARA BURGERHARTSTRAAT 25, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS},
	pages = {1319-1323},
	publisher = {Elsevier Science Bv},
	organization = {Elsevier Science Bv},
	address = {Amsterdam},
	abstract = {A common misconception is that X-ray diffraction is the best way to measure bond distances. However, in some cases where disorder is present it can yield incorrect answers. The silicon-fluoride bond distance in fluoride-containing zeolite SFF has been measured using two magic angle spinning NMR techniques. Both techniques, variable contact time cross polarization and spinning side hand intensity fitting give shorter Si-F bond distances than X-ray diffraction.},
	keywords = {5-COORDINATE SILICON, COMPLEX, IFR, IONS, LOCATION, MEDIA, MOLECULAR-SIEVES, SOLID-STATE NMR, STF, TEMPLATE},
	isbn = {0167-29910-444-51805-3},
	url = {<Go to ISI>://000227357201022},
	author = {Darton, R. J. and Brouwer, D. H. and Fyfe, C. A. and Villaescusa, L. A. and Morris, R. E.},
	editor = {VanSteen, E. and Claeys, M. and Callanan, L. H.}
}
@article {834,
	title = {Solid-state NMR studies of the fluoride-containing zeolite SSZ-44},
	journal = {Chemistry of Materials},
	volume = {16},
	number = {4},
	year = {2004},
	note = {ISI Document Delivery No.: 774YATimes Cited: 12Cited Reference Count: 21},
	month = {Feb},
	pages = {600-603},
	type = {Article},
	abstract = {Magic-angle spinning NMR has been used to probe the local structure of as-made zeolite SFF containing occluded fluoride and NN-diethyl-2,6-dimethylpiperidinium. The Si-F bond distance has been measured using two methods: variable contact time cross polarization studies (1.74 Angstrom) and spinning sideband intensity fitting at relatively slow spinning speeds (1.79 Angstrom). Both measurements yield results that are significantly shorter than the internuclear Si-F distance as measured by single-crystal X-ray diffraction (similar to1.9 Angstrom), which is based on the average positions of the atoms due to disorder and hence does not reflect the true bond distance.},
	keywords = {5-COORDINATE SILICON, COMPLEX, IFR, IONS, LOCATION, MEDIA, MOLECULAR-SIEVES, SPECTROSCOPY, STF, TEMPLATE},
	isbn = {0897-4756},
	url = {<Go to ISI>://000189012900008},
	author = {Darton, R. J. and Brouwer, D. H. and Fyfe, C. A. and Villaescusa, L. A. and Morris, R. E.}
}
@inbook {654,
	title = {Synthesis of poly(N,N-dimethylacrylamide) brushes from functionalized latex surfaces by aqueous atom transfer radical polymerization},
	booktitle = {Advances in Controlled/Living Radical Polymerization},
	series = {Acs Symposium Series},
	volume = {854},
	year = {2003},
	note = {ISI Document Delivery No.: BW85KTimes Cited: 7Cited Reference Count: 30Proceedings Paper224th National Meeting of the American-Chemical-SocietyAUG 17-22, 2002BOSTON, MASSACHUSETTSAmer Chem Soc1155 SIXTEENTH ST NW, WASHINGTON, DC 20036 USA},
	pages = {316-330},
	publisher = {Amer Chemical Soc},
	organization = {Amer Chemical Soc},
	address = {Washington},
	abstract = {Negatively charged, ATRP initiator functionalized polystyrene latexes were synthesized and N,N-dimethylacrylamide was polymerized from their surfaces by aqueous ATRP using several catalyst combinations. Very high grafting densities and molecular weights were achieved with good polydispersities. The brushes exhibited a strong repulsive force that increased with molecular weight in atomic force microscopy measurements. Hydrodynamic thicknesses were consistent with theory. Polymerization from these surfaces is very different from ATRP in solution and depends on monomer concentration in solution, type of catalyst, and surface initiator concentration. The observations were explained with an electrostatic model of the surface region that predicts an increase in the local concentration of Cu(I) and Cu(II) catalyst complexes.},
	keywords = {ADSORPTION, BLOCK-COPOLYMERS, density, FORCE MICROSCOPE, INITIATED POLYMERIZATIONS, LAYER, MEDIA, POLYMERS, SELF-ASSEMBLED MONOLAYERS},
	isbn = {0097-61560-8412-3854-5},
	url = {<Go to ISI>://000183406500022},
	author = {Kizhakkedathu, J. N. and Goodman, D. and Brooks, D. E.},
	editor = {Matyjaszewski, K.}
}
@article {425,
	title = {A F-19 nuclear magnetic resonance study of the conjugate Bronsted-Lewis superacid HSO3F-SbF5. Part II},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {80},
	number = {9},
	year = {2002},
	note = {ISI Document Delivery No.: 607YFTimes Cited: 4Cited Reference Count: 31},
	month = {Sep},
	pages = {1265-1277},
	type = {Article},
	abstract = {Solutions of SbF5 in HSO3F with x(SbF5) = 0.012 to 0.405 are studied by 500 MHz H-1 NMR (299 K) and 471 MHz F-19 NMR (213-250 K), using NMR tubes fitted with fluoropolymer lining. The initial process during dissolution is the fast solvolysis of monomeric SbF5 in HSO3F according to SbF5 + nHSO(3)F left arrow SbF5 - n(SO3F)(n) + nHF (n = 1, 2). All HF formed during solvolysis will no longer be removed by reaction with glass, but will remain in the superacid system. Besides participation in the fast formation of various fluoro-fluorosulfato anions [SbF6 - n(SO3F)(n)](-) (n = 0, 1, 2) and acidium ions [H2X](+)((solv.)) (X= F, SO3F), HF is involved in slow-exchange reactions of the type [SbF6 - n(SO3F)(n)](-)((solv.)) + HF left arrow [SbF7 - n(SO3F)(n- 1)](-)((solv.)) + HSO3F (n = 1, 2) detected because of a delay of 3 months between sample preparation and measurements and confirmed by repeating theses measurements after a further 3 months. There are three notable differences to our earlier study, affecting concentrations of the fluoro-fluorosulfato antimonate anions observed: (i) in dilute solutions [SbF6](-) is formed in high concentrations (34.7-76.1\%), with [Sb2F11](-) now clearly detected at intermediate to high SbF5 concentrations (up to 5.8\%); (ii) bis-fluorosulfato anions (cis-, trans-[SbF4(SO3F)(2)](-)) are found in much lower concentrations only, which decrease further with time, while tris-fluorosulfato anions ([SbF3(SO3F)(3)](-)) are now no longer observed; (iii) these reduced concentrations of poly-fluorosulfato anions in dilute solutions are responsible for the formation of fewer mu-SO3F-oligomers at lower concentrations, when more SbF5 is added. As a consequence, the HSO3F-SbF5 magic acid system is now less complex than found previously and only seven anionic species are clearly observed.},
	keywords = {ANTIMONY PENTAFLUORIDE, antimony(V) fluoroanions, F-19 NMR, H-1 NMR, HF-SBF5, MEDIA, RELATIVE ACIDITY, SBF5, solvolysis, superacids, SYSTEMS},
	isbn = {0008-4042},
	url = {<Go to ISI>://000178817800011},
	author = {Kuhn-Velten, J. and Bodenbinder, M. and Brochler, R. and Hagele, G. and Aubke, F.}
}
@article {5087,
	title = {Host-guest binding of simple cavitands in water},
	journal = {Chemical Communications},
	number = {24},
	year = {2001},
	note = {ISI Document Delivery No.: 507TGTimes Cited: 15Cited Reference Count: 37},
	month = {Dec},
	pages = {2680-2681},
	type = {Article},
	abstract = {Simple water soluble cavitands were prepared and the thermodynamics of their binding with neutral guests in water is reported.},
	keywords = {AQUEOUS-SOLUTION, COMPLEXATION, ERROR PROPAGATION, INDUCED-FIT, MEDIA, molecular recognition, MONTE-CARLO SIMULATION, NMR CHEMICAL-SHIFTS, RECTANGULAR HYPERBOLAE, SOLUBLE RESORCIN<4>ARENE},
	isbn = {1359-7345},
	url = {<Go to ISI>://000173044900077},
	author = {Gui, X. and Sherman, J. C.}
}
@article {4763,
	title = {Latent chemical behavior revealed in the crystalline state: novel photochemistry of a cis-9-decalyl aryl ketone},
	journal = {Chemical Communications},
	number = {23},
	year = {2000},
	note = {ISI Document Delivery No.: 376ZLTimes Cited: 6Cited Reference Count: 12},
	pages = {2309-2310},
	type = {Article},
	abstract = {The case of a ketone whose photochemistry in solution is markedly different from that observed in the crystalline state is reported.},
	keywords = {HYDROGEN ATOM ABSTRACTION, II REACTION, MEDIA},
	isbn = {1359-7345},
	url = {<Go to ISI>://000165487300010},
	author = {Cheung, E. and Kang, T. and Scheffer, J. R. and Trotter, J.}
}
@article {4763,
	title = {Latent chemical behavior revealed in the crystalline state: novel photochemistry of a cis-9-decalyl aryl ketone},
	journal = {Chemical Communications},
	number = {23},
	year = {2000},
	note = {ISI Document Delivery No.: 376ZLTimes Cited: 6Cited Reference Count: 12},
	pages = {2309-2310},
	type = {Article},
	abstract = {The case of a ketone whose photochemistry in solution is markedly different from that observed in the crystalline state is reported.},
	keywords = {HYDROGEN ATOM ABSTRACTION, II REACTION, MEDIA},
	isbn = {1359-7345},
	url = {<Go to ISI>://000165487300010},
	author = {Cheung, E. and Kang, T. and Scheffer, J. R. and Trotter, J.}
}
@article {4554,
	title = {Computational prediction of the enantioselectivity of a solid-state photoreaction},
	journal = {Organic Letters},
	volume = {1},
	number = {8},
	year = {1999},
	note = {ISI Document Delivery No.: 281QKTimes Cited: 8Cited Reference Count: 26},
	month = {Oct},
	pages = {1279-1281},
	type = {Article},
	abstract = {[GRAPHICS] To better understand the forces controlling chemical reactions in crystals, the absolute asymmetric photorearrangement of 4-m-chlorobenzyloxy-2-pyridone leading to the corresponding enantiomerically enriched (78\% ee) beta-lactam was modeled computationally using a flexible minilattice consisting of a central reactant and 20 nearest and 72 next-nearest neighbors. The computational results predicted a preference for formation of the (R,R)-enantiomer, and this was verified experimentally by absolute configuration correlation studies.},
	keywords = {ABSOLUTE ASYMMETRIC-SYNTHESIS, CRYSTAL LATTICES, FORCE-FIELD, MEDIA, MODEL, MOLECULAR MECHANICS, NUCLEIC-ACIDS, PHOTOCHEMISTRY, PROTEINS},
	isbn = {1523-7060},
	url = {<Go to ISI>://000085172100037},
	author = {Garcia-Garibay, M. A. and Houk, K. N. and Keating, A. E. and Cheer, C. J. and Leibovitch, M. and Scheffer, J. R. and Wu, L. C.}
}
@article {4713,
	title = {A F-19 nuclear magnetic resonance study of the conjugate Bronsted-Lewis superacid HSO3F-SbF5. Part 1},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {77},
	number = {11},
	year = {1999},
	note = {ISI Document Delivery No.: 253FETimes Cited: 5Cited Reference Count: 32},
	month = {Nov},
	pages = {1869-1886},
	type = {Article},
	abstract = {The Bronsted-Lewis superacid HSO3F-SbF5 or "magic acid" is re-investigated by modern F-19 NMR methods over a wide concentration range. The system is found to be considerably more complex than had been assumed previously. A,total of 13 different anions are identified of which only five have previously been identified in magic acid. With increasing SbF5 contents the concentration of monomeric anions like [SbF6](-), [SbF5(SO3F)](-), cis- and trans-[SbF4(SO3F)(2)](-), and mer-[SbF3(SO3F)(3)](-) gradually decreases. Except for [Sb2F11](-), which is present in very small concentrations only the formation of oligomers involves exclusively mu-fluorosulfato bridges. In addition to donor (SO3F)(-) and acceptor (SbF5) complex formation to give [SbF5(SO3F)](-) and possibly ligand redistribution, the solvolysis of SbF5 or SbF4(SO3F) in HSO3F appears to be the principal formation reaction for polyfluorosulfatofluoroantimonate(V) anions. In glass (NMR tubes) the solvolysis product HF is converted to the oxonium ion [H3O](+), which has previously been identified by H-1 NMR and structurally characterized as [H3O][Sb2F11] by us.},
	keywords = {ANTIMONY PENTAFLUORIDE, conjugate superacid, F-19 NMR spectra, FLUOROSULFATE, fluorosulfuric acid, HF-SBF5, magic acid, MEDIA, RELATIVE ACIDITY, SBF5, SYSTEMS},
	isbn = {0008-4042},
	url = {<Go to ISI>://000083545300020},
	author = {Zhang, D. L. and Heubes, M. and Hagele, G. and Aubke, F.}
}
@article {4208,
	title = {Analyte-additive interactions in nonaqueous capillary electrophoresis: a critical review},
	journal = {Trac-Trends in Analytical Chemistry},
	volume = {17},
	number = {7},
	year = {1998},
	note = {ISI Document Delivery No.: 107HPTimes Cited: 54Cited Reference Count: 40},
	month = {Aug},
	pages = {424-434},
	type = {Review},
	abstract = {This article reviews the recent developments in nonaqueous capillary electrophoresis and discusses the effect of the solvent on analyte-additive interactions. When nonaqueous solvents are used, solvophobic interactions are generally weaker than those in water; therefore, those additives that can change the analyte mobility through electrostatic or donor-acceptor interactions should be further explored. (C) 1998 Elsevier Science B.V. All rights reserved.},
	keywords = {ANIONS, CHIRAL SEPARATION, cohesion energy, density, dielectric constant, electron donor-acceptor interaction, FORMAMIDE, ION, MEDIA, nonaqueous capillary electrophoresis, SEPARATION SELECTIVITY, solvent effect, SOLVENTS, SURFACTANTS, WATER, ZONE ELECTROPHORESIS},
	isbn = {0165-9936},
	url = {<Go to ISI>://000075202300022},
	author = {Bowser, M. T. and Kranack, A. R. and Chen, D. D. Y.}
}
