@article {2344,
	title = {Tuning Gold Nanoparticle Self-Assembly for Optimum Coherent Anti-Stokes Raman Scattering and Second Harmonic Generation Response},
	journal = {Journal of Physical Chemistry C},
	volume = {113},
	number = {9},
	year = {2009},
	note = {ISI Document Delivery No.: 412ODTimes Cited: 3Cited Reference Count: 66Addison, Christopher J. Konorov, Stanislav O. Brolo, Alexandre G. Blades, Michael W. Turner, Robin F. B.},
	month = {Mar},
	pages = {3586-3592},
	type = {Article},
	abstract = {The research and development of new substrates for use in surface-enhanced spectroscopy is primarily motivated by the ability to tune such substrates to provide maximum signal enhancement and therefore lower detection limits. We examined a series of multilayer nanoparticle (NP) arrays with between 1 and 17 NP layers using two nonlinear optical (NLO) techniques: Coherent anti-Stokes Raman scattering (CARS) and second harmonic generation (SHG). The CARS signal of oxazine 720 was monitored at 1600 cm(-1) using a 709-nm pump beam and an 800-nm stokes beam. Maximum signal was observed for 11 NP layers and is attributed to the matching of the CARS signal and the substrate surface plasmon excitation at 637 nm. The CARS signal for the 3000-cm(-1) C-H stretching vibration showed maximum enhancement at 13 NP layers. The maximum SHG signal enhancement occurred at 13 NP layers, with a 50-fold overall enhancement of the SHG signal. We demonstrate that the NP-containing substrates can be tuned to provide maximum NLO response based on the number of NP depositions and the wavelength(s) involved in the NLO experiments. These multilayer NP arrays yield a stable and modular spectroscopic substrate advantageous for a variety of surface-enhanced spectroscopic techniques.},
	keywords = {ABSORPTION, ARRAYS, AU-COLLOID, BROKEN SYMMETRY, ENHANCEMENT, FILMS, HARMONIC-GENERATION, MONOLAYERS, NONLINEAR-OPTICAL RESPONSES, SPECTROSCOPY, SURFACE-PLASMON RESONANCE},
	isbn = {1932-7447},
	url = {<Go to ISI>://000263733200034},
	author = {Addison, C. J. and Konorov, S. O. and Brolo, A. G. and Blades, M. W. and Turner, R. F. B.}
}
@article {2344,
	title = {Tuning Gold Nanoparticle Self-Assembly for Optimum Coherent Anti-Stokes Raman Scattering and Second Harmonic Generation Response},
	journal = {Journal of Physical Chemistry C},
	volume = {113},
	number = {9},
	year = {2009},
	note = {ISI Document Delivery No.: 412ODTimes Cited: 3Cited Reference Count: 66Addison, Christopher J. Konorov, Stanislav O. Brolo, Alexandre G. Blades, Michael W. Turner, Robin F. B.},
	month = {Mar},
	pages = {3586-3592},
	type = {Article},
	abstract = {The research and development of new substrates for use in surface-enhanced spectroscopy is primarily motivated by the ability to tune such substrates to provide maximum signal enhancement and therefore lower detection limits. We examined a series of multilayer nanoparticle (NP) arrays with between 1 and 17 NP layers using two nonlinear optical (NLO) techniques: Coherent anti-Stokes Raman scattering (CARS) and second harmonic generation (SHG). The CARS signal of oxazine 720 was monitored at 1600 cm(-1) using a 709-nm pump beam and an 800-nm stokes beam. Maximum signal was observed for 11 NP layers and is attributed to the matching of the CARS signal and the substrate surface plasmon excitation at 637 nm. The CARS signal for the 3000-cm(-1) C-H stretching vibration showed maximum enhancement at 13 NP layers. The maximum SHG signal enhancement occurred at 13 NP layers, with a 50-fold overall enhancement of the SHG signal. We demonstrate that the NP-containing substrates can be tuned to provide maximum NLO response based on the number of NP depositions and the wavelength(s) involved in the NLO experiments. These multilayer NP arrays yield a stable and modular spectroscopic substrate advantageous for a variety of surface-enhanced spectroscopic techniques.},
	keywords = {ABSORPTION, ARRAYS, AU-COLLOID, BROKEN SYMMETRY, ENHANCEMENT, FILMS, HARMONIC-GENERATION, MONOLAYERS, NONLINEAR-OPTICAL RESPONSES, SPECTROSCOPY, SURFACE-PLASMON RESONANCE},
	isbn = {1932-7447},
	url = {<Go to ISI>://000263733200034},
	author = {Addison, C. J. and Konorov, S. O. and Brolo, A. G. and Blades, M. W. and Turner, R. F. B.}
}
@article {4903,
	title = {Improved synthesis of isogranulatimide, a G2 checkpoint inhibitor. Syntheses of didemnimide C, isodidemnimide A, neodidemnimide A, 17-methylgranulatimide, and isogranulatimides A-C},
	journal = {Journal of Organic Chemistry},
	volume = {65},
	number = {2},
	year = {2000},
	note = {ISI Document Delivery No.: 276YFTimes Cited: 44Cited Reference Count: 35},
	month = {Jan},
	pages = {530-535},
	type = {Article},
	abstract = {A concise, improved synthesis of isogranulatimide (6), a naturally occurring substance with G2 checkpoint inhibition activity, is described. Also reported are the syntheses of didemnimide C (18), isodidemnimide A (24), neodidemnimide A (36), 17-methylgranulatimide (9), and isogranulatimides A (10), B (11), and C (12). Compounds 9-12, congeners of isogranulatimide (6), are now available for biological evaluation.},
	keywords = {BHK CELLS, CAFFEINE, CANCER, CELL-CYCLE CHECKPOINTS, CISPLATIN, DERIVATIVES, DNA-REPLICATION, ENHANCEMENT, IMIDAZOLES, RADIOSENSITIZATION},
	isbn = {0022-3263},
	url = {<Go to ISI>://000084905400039},
	author = {Piers, E. and Britton, R. and Andersen, R. J.}
}
@article {3338,
	title = {INEPT EXPERIMENTS IN SOLID-STATE NMR},
	journal = {Journal of the American Chemical Society},
	volume = {117},
	number = {41},
	year = {1995},
	note = {ISI Document Delivery No.: TB353Times Cited: 38Cited Reference Count: 16},
	month = {Oct},
	pages = {10397-10398},
	type = {Note},
	keywords = {DOUBLE-RESONANCE NMR, ENHANCEMENT, HELICAL PEPTIDE, INTERATOMIC DISTANCE, NUCLEI, POLARIZATION TRANSFER, QUADRUPOLAR, REDOR, SIGNALS, VPI-5},
	isbn = {0002-7863},
	url = {<Go to ISI>://A1995TB35300031},
	author = {Fyfe, C. A. and Wongmoon, K. C. and Huang, Y. and Grondey, H.}
}
@article {3118,
	title = {PORPHYRIN CHEMISTRY PERTAINING TO THE DESIGN OF ANTICANCER DRUGS .2. THE SYNTHESIS AND IN-VITRO TESTS OF WATER-SOLUBLE PORPHYRINS CONTAINING, IN THE MESO POSITIONS, THE FUNCTIONAL-GROUPS - 4-METHYLPYRIDINIUM, OR 4-SULFONATOPHENYL, IN COMBINATION WITH PHEN},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {72},
	number = {12},
	year = {1994},
	note = {ISI Document Delivery No.: QC582Times Cited: 38Cited Reference Count: 46},
	month = {Dec},
	pages = {2447-2457},
	type = {Article},
	abstract = {Water-soluble, meso-substituted porphyrins are synthesized by sulfonation or methylation of the phenyl or pyridyl groups, respectively, of some non-water-soluble functionalized porphyrins that we have recently synthesized (Can. J. Chem. 72, 1894 (1994)). Twelve anionic sulfonated and seven cationic methylpyridinium porphyrins, usually containing other functional groups (phenyl, pyridyl, nitro- and amino-phenyl), are reported on. Twelve of these porphyrins are new, and all nineteen porphyrins are characterized by H-1 NMR. UV-VIS data are presented for the isolated porphyrins, while mass spectral data are noted for selected compounds. Partition coefficients of the porphyrins in octanol-water, and the accumulation of the porphyrins in HT-29 cells of a human-cancer tumor, were measured and both were inversely related to the charges of the porphyrins. The 11 porphyrins soluble in biological buffer solutions are basically nontoxic to Chinese hamster ovary (CHO) cells in oxic or hypoxic conditions or to aerobic HT-29 cells at the 100 mu M concentration used (which is sometimes limited by solubility). No significant X-ray radiosensitization was observed for selected porphyrins toward CHO cells at the 100 mu M concentrations used, but some photosensitized cell kill (using 630 nm light) was observed using the disodium salt of 5,10-bis(4-pyridyl)-15,20-bis(4-sulfonatophenyl)porphyrin (24).},
	keywords = {AGGREGATION, CATIONIC PORPHYRIN, CELLULAR DELIVERY, COMPLEXES, DERIVATIVES, DNA, ENHANCEMENT, INTERCALATION, METALLOPORPHYRINS, PHOTOSENSITIZATION},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1994QC58200011},
	author = {Meng, G. G. and James, Brian R. and Skov, K. A. and Korbelik, M.}
}
