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Gender Differences in Marital Status Moderation of Genetic and Environmental Influences on Subjective Health.

Behavior genetics

Finkel D, Franz CE, Horwitz B, Christensen K, Gatz M, Johnson W, Kaprio J, Korhonen T, Niederheiser J, Petersen I, Rose RJ, Silventoinen K.
PMID: 26468112
Behav Genet. 2016 Jan;46:114-123. doi: 10.1007/s10519-015-9758-y. Epub 2015 Oct 14.

From the IGEMS Consortium, data were available from 26,579 individuals aged 23 to 102 years on 3 subjective health items: self-rated health (SRH), health compared to others (COMP), and impact of health on activities (ACT). Marital status was a...

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Finkel D, Franz CE, Horwitz B, et al. Gender Differences in Marital Status Moderation of Genetic and Environmental Influences on Subjective Health. Behav Genet. 2015;46:114-123doi: 10.1007/s10519-015-9758-y.
Finkel, D., Franz, C. E., Horwitz, B., Christensen, K., Gatz, M., Johnson, W., Kaprio, J., Korhonen, T., Niederheiser, J., Petersen, I., Rose, R. J., & Silventoinen, K. (2016). Gender Differences in Marital Status Moderation of Genetic and Environmental Influences on Subjective Health. Behavior genetics, 46114-123. https://doi.org/10.1007/s10519-015-9758-y
Finkel, Deborah, et al. "Gender Differences in Marital Status Moderation of Genetic and Environmental Influences on Subjective Health." Behavior genetics vol. 46 (2016): 114-123. doi: https://doi.org/10.1007/s10519-015-9758-y
Finkel D, Franz CE, Horwitz B, Christensen K, Gatz M, Johnson W, Kaprio J, Korhonen T, Niederheiser J, Petersen I, Rose RJ, Silventoinen K. Gender Differences in Marital Status Moderation of Genetic and Environmental Influences on Subjective Health. Behav Genet. 2016 Jan;46:114-123. doi: 10.1007/s10519-015-9758-y. Epub 2015 Oct 14. PMID: 26468112; PMCID: PMC4833715.
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Is it homogeneous or heterogeneous catalysis? Identification of bulk ruthenium metal as the true catalyst in benzene hydrogenations starting with the monometallic precursor, Ru(II)(eta 6-C6Me6)(OAc)2, plus kinetic characterization of the heterogeneous nucleation, then autocatalytic surface-growth mechanism of metal film formation.

Journal of the American Chemical Society

Widegren JA, Bennett MA, Finke RG.
PMID: 12926954
J Am Chem Soc. 2003 Aug 27;125(34):10301-10. doi: 10.1021/ja021436c.

A reinvestigation of the true catalyst in a benzene hydrogenation system beginning with Ru(II)(eta(6)-C(6)Me(6))(OAc)(2) as the precatalyst is reported. The key observations leading to the conclusion that the true catalyst is bulk ruthenium metal particles, and not a homogeneous...

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Widegren JA, Bennett MA, Finke RG. Is it homogeneous or heterogeneous catalysis? Identification of bulk ruthenium metal as the true catalyst in benzene hydrogenations starting with the monometallic precursor, Ru(II)(eta 6-C6Me6)(OAc)2, plus kinetic characterization of the heterogeneous nucleation, then autocatalytic surface-growth mechanism of metal film formation. J Am Chem Soc. 2003;125(34):10301-10doi: 10.1021/ja021436c.
Widegren, J. A., Bennett, M. A., & Finke, R. G. (2003). Is it homogeneous or heterogeneous catalysis? Identification of bulk ruthenium metal as the true catalyst in benzene hydrogenations starting with the monometallic precursor, Ru(II)(eta 6-C6Me6)(OAc)2, plus kinetic characterization of the heterogeneous nucleation, then autocatalytic surface-growth mechanism of metal film formation. Journal of the American Chemical Society, 125(34), 10301-10. https://doi.org/10.1021/ja021436c
Widegren, Jason A, et al. "Is it homogeneous or heterogeneous catalysis? Identification of bulk ruthenium metal as the true catalyst in benzene hydrogenations starting with the monometallic precursor, Ru(II)(eta 6-C6Me6)(OAc)2, plus kinetic characterization of the heterogeneous nucleation, then autocatalytic surface-growth mechanism of metal film formation." Journal of the American Chemical Society vol. 125,34 (2003): 10301-10. doi: https://doi.org/10.1021/ja021436c
Widegren JA, Bennett MA, Finke RG. Is it homogeneous or heterogeneous catalysis? Identification of bulk ruthenium metal as the true catalyst in benzene hydrogenations starting with the monometallic precursor, Ru(II)(eta 6-C6Me6)(OAc)2, plus kinetic characterization of the heterogeneous nucleation, then autocatalytic surface-growth mechanism of metal film formation. J Am Chem Soc. 2003 Aug 27;125(34):10301-10. doi: 10.1021/ja021436c. PMID: 12926954.
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Iridium(0) nanocluster, acid-assisted catalysis of neat acetone hydrogenation at room temperature: exceptional activity, catalyst lifetime, and selectivity at complete conversion.

Journal of the American Chemical Society

Ozkar S, Finke RG.
PMID: 15796546
J Am Chem Soc. 2005 Apr 06;127(13):4800-8. doi: 10.1021/ja0437813.

Acetone hydrogenation catalysis is important in applications such as heat pumps and fuel cells or in fulfilling the sizable demand for the product of selective acetone hydrogenation, 2-propanol. Reported herein is the discovery of a superior acetone hydrogenation catalyst--superior...

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Ozkar S, Finke RG. Iridium(0) nanocluster, acid-assisted catalysis of neat acetone hydrogenation at room temperature: exceptional activity, catalyst lifetime, and selectivity at complete conversion. J Am Chem Soc. 2005;127(13):4800-8doi: 10.1021/ja0437813.
Ozkar, S., & Finke, R. G. (2005). Iridium(0) nanocluster, acid-assisted catalysis of neat acetone hydrogenation at room temperature: exceptional activity, catalyst lifetime, and selectivity at complete conversion. Journal of the American Chemical Society, 127(13), 4800-8. https://doi.org/10.1021/ja0437813
Ozkar, Saim, and Finke, Richard G. "Iridium(0) nanocluster, acid-assisted catalysis of neat acetone hydrogenation at room temperature: exceptional activity, catalyst lifetime, and selectivity at complete conversion." Journal of the American Chemical Society vol. 127,13 (2005): 4800-8. doi: https://doi.org/10.1021/ja0437813
Ozkar S, Finke RG. Iridium(0) nanocluster, acid-assisted catalysis of neat acetone hydrogenation at room temperature: exceptional activity, catalyst lifetime, and selectivity at complete conversion. J Am Chem Soc. 2005 Apr 06;127(13):4800-8. doi: 10.1021/ja0437813. PMID: 15796546.
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Nanocluster formation and stabilization fundamental studies: investigating "solvent-only" stabilization en route to discovering stabilization by the traditionally weakly coordinating anion BF4- plus high dielectric constant solvents.

Inorganic chemistry

Ott LS, Finke RG.
PMID: 16999438
Inorg Chem. 2006 Oct 02;45(20):8382-93. doi: 10.1021/ic060876s.

The nanocluster literature contains a wide variety of nanocluster stabilizing agents. In addition to the plethora of putative stabilizing additives, 12 claims appear of "solvent-only" stabilization of transition-metal nanoclusters-a hypothesis that is tested for the first time as part...

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Ott LS, Finke RG. Nanocluster formation and stabilization fundamental studies: investigating "solvent-only" stabilization en route to discovering stabilization by the traditionally weakly coordinating anion BF4- plus high dielectric constant solvents. Inorg Chem. 2006;45(20):8382-93doi: 10.1021/ic060876s.
Ott, L. S., & Finke, R. G. (2006). Nanocluster formation and stabilization fundamental studies: investigating "solvent-only" stabilization en route to discovering stabilization by the traditionally weakly coordinating anion BF4- plus high dielectric constant solvents. Inorganic chemistry, 45(20), 8382-93. https://doi.org/10.1021/ic060876s
Ott, Lisa Starkey, and Finke, Richard G. "Nanocluster formation and stabilization fundamental studies: investigating "solvent-only" stabilization en route to discovering stabilization by the traditionally weakly coordinating anion BF4- plus high dielectric constant solvents." Inorganic chemistry vol. 45,20 (2006): 8382-93. doi: https://doi.org/10.1021/ic060876s
Ott LS, Finke RG. Nanocluster formation and stabilization fundamental studies: investigating "solvent-only" stabilization en route to discovering stabilization by the traditionally weakly coordinating anion BF4- plus high dielectric constant solvents. Inorg Chem. 2006 Oct 02;45(20):8382-93. doi: 10.1021/ic060876s. PMID: 16999438.
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Research management. Protests by staff, advisers rattle Australian Synchrotron.

Science (New York, N.Y.)

Finkel E.
PMID: 20044547
Science. 2010 Jan 01;327(5961):20-1. doi: 10.1126/science.327.5961.20.

No abstract available.

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Finkel E. Research management. Protests by staff, advisers rattle Australian Synchrotron. Science. 2010;327(5961):20-1doi: 10.1126/science.327.5961.20.
Finkel, E. (2010). Research management. Protests by staff, advisers rattle Australian Synchrotron. Science (New York, N.Y.), 327(5961), 20-1. https://doi.org/10.1126/science.327.5961.20
Finkel, Elizabeth. "Research management. Protests by staff, advisers rattle Australian Synchrotron." Science (New York, N.Y.) vol. 327,5961 (2010): 20-1. doi: https://doi.org/10.1126/science.327.5961.20
Finkel E. Research management. Protests by staff, advisers rattle Australian Synchrotron. Science. 2010 Jan 01;327(5961):20-1. doi: 10.1126/science.327.5961.20. PMID: 20044547.
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Asymptotic statistical theory of overtraining and cross-validation.

IEEE transactions on neural networks

Amari S, Murata N, Muller KR, Finke M, Yang HH.
PMID: 18255701
IEEE Trans Neural Netw. 1997;8(5):985-96. doi: 10.1109/72.623200.

A statistical theory for overtraining is proposed. The analysis treats general realizable stochastic neural networks, trained with Kullback-Leibler divergence in the asymptotic case of a large number of training examples. It is shown that the asymptotic gain in the...

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Amari S, Murata N, Muller KR, et al. Asymptotic statistical theory of overtraining and cross-validation. IEEE Trans Neural Netw. 1997;8(5):985-96doi: 10.1109/72.623200.
Amari, S., Murata, N., Muller, K. R., Finke, M., & Yang, H. H. (1997). Asymptotic statistical theory of overtraining and cross-validation. IEEE transactions on neural networks, 8(5), 985-96. https://doi.org/10.1109/72.623200
Amari, S, et al. "Asymptotic statistical theory of overtraining and cross-validation." IEEE transactions on neural networks vol. 8,5 (1997): 985-96. doi: https://doi.org/10.1109/72.623200
Amari S, Murata N, Muller KR, Finke M, Yang HH. Asymptotic statistical theory of overtraining and cross-validation. IEEE Trans Neural Netw. 1997;8(5):985-96. doi: 10.1109/72.623200. PMID: 18255701.
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Transition-metal nanocluster size vs formation time and the catalytically effective nucleus number: a mechanism-based treatment.

Journal of the American Chemical Society

Watzky MA, Finney EE, Finke RG.
PMID: 18707099
J Am Chem Soc. 2008 Sep 10;130(36):11959-69. doi: 10.1021/ja8017412. Epub 2008 Aug 16.

A mechanism-based equation for the size of a forming transition-metal nanocluster vs time has been derived based on the Finke-Watzky two-step mechanism for transition-metal nanocluster nucleation (A --> B, rate constant k1) and autocatalytic growth (A + B -->...

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Watzky MA, Finney EE, Finke RG. Transition-metal nanocluster size vs formation time and the catalytically effective nucleus number: a mechanism-based treatment. J Am Chem Soc. 2008;130(36):11959-69doi: 10.1021/ja8017412.
Watzky, M. A., Finney, E. E., & Finke, R. G. (2008). Transition-metal nanocluster size vs formation time and the catalytically effective nucleus number: a mechanism-based treatment. Journal of the American Chemical Society, 130(36), 11959-69. https://doi.org/10.1021/ja8017412
Watzky, Murielle A, et al. "Transition-metal nanocluster size vs formation time and the catalytically effective nucleus number: a mechanism-based treatment." Journal of the American Chemical Society vol. 130,36 (2008): 11959-69. doi: https://doi.org/10.1021/ja8017412
Watzky MA, Finney EE, Finke RG. Transition-metal nanocluster size vs formation time and the catalytically effective nucleus number: a mechanism-based treatment. J Am Chem Soc. 2008 Sep 10;130(36):11959-69. doi: 10.1021/ja8017412. Epub 2008 Aug 16. PMID: 18707099.
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Platinum-catalyzed phenyl and methyl group transfer from tin to iridium: evidence for an autocatalytic reaction pathway with an unusual preference for methyl transfer.

Journal of the American Chemical Society

Smith SE, Sasaki JM, Bergman RG, Mondloch JE, Finke RG.
PMID: 18198879
J Am Chem Soc. 2008 Feb 13;130(6):1839-41. doi: 10.1021/ja710365x. Epub 2008 Jan 17.

No abstract available.

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Smith SE, Sasaki JM, Bergman RG, et al. Platinum-catalyzed phenyl and methyl group transfer from tin to iridium: evidence for an autocatalytic reaction pathway with an unusual preference for methyl transfer. J Am Chem Soc. 2008;130(6):1839-41doi: 10.1021/ja710365x.
Smith, S. E., Sasaki, J. M., Bergman, R. G., Mondloch, J. E., & Finke, R. G. (2008). Platinum-catalyzed phenyl and methyl group transfer from tin to iridium: evidence for an autocatalytic reaction pathway with an unusual preference for methyl transfer. Journal of the American Chemical Society, 130(6), 1839-41. https://doi.org/10.1021/ja710365x
Smith, Stuart E, et al. "Platinum-catalyzed phenyl and methyl group transfer from tin to iridium: evidence for an autocatalytic reaction pathway with an unusual preference for methyl transfer." Journal of the American Chemical Society vol. 130,6 (2008): 1839-41. doi: https://doi.org/10.1021/ja710365x
Smith SE, Sasaki JM, Bergman RG, Mondloch JE, Finke RG. Platinum-catalyzed phenyl and methyl group transfer from tin to iridium: evidence for an autocatalytic reaction pathway with an unusual preference for methyl transfer. J Am Chem Soc. 2008 Feb 13;130(6):1839-41. doi: 10.1021/ja710365x. Epub 2008 Jan 17. PMID: 18198879.
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1-Bromo-methyl-4-aza-1-azoniabicyclo-[2.2.2]octane bromide.

Acta crystallographica. Section E, Structure reports online

Finke AD, Gray DL, Moore JS.
PMID: 21579799
Acta Crystallogr Sect E Struct Rep Online. 2010 Jan 16;66:o377. doi: 10.1107/S1600536810000292.

The title compound, C(7)H(14)BrN(2) (+)·Br(-), was prepared by nucleophilic substitution of DABCO (systematic name: 1,4-diaza-bicyclo-[2.2.2]octa-ne) with dibromo-methane in acetone. The structure features Br⋯H close contacts (2.79 and 2.90 Å) as well as a weak bromine-bromide inter-action [3.6625 (6) Å].

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Finke AD, Gray DL, Moore JS. 1-Bromo-methyl-4-aza-1-azoniabicyclo-[2.2.2]octane bromide. Acta Crystallogr Sect E Struct Rep Online. 2010;66:o377doi: 10.1107/S1600536810000292.
Finke, A. D., Gray, D. L., & Moore, J. S. (2010). 1-Bromo-methyl-4-aza-1-azoniabicyclo-[2.2.2]octane bromide. Acta crystallographica. Section E, Structure reports online, 66o377. https://doi.org/10.1107/S1600536810000292
Finke, Aaron D, et al. "1-Bromo-methyl-4-aza-1-azoniabicyclo-[2.2.2]octane bromide." Acta crystallographica. Section E, Structure reports online vol. 66 (2010): o377. doi: https://doi.org/10.1107/S1600536810000292
Finke AD, Gray DL, Moore JS. 1-Bromo-methyl-4-aza-1-azoniabicyclo-[2.2.2]octane bromide. Acta Crystallogr Sect E Struct Rep Online. 2010 Jan 16;66:o377. doi: 10.1107/S1600536810000292. PMID: 21579799; PMCID: PMC2979768.
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Equimolar CO(2) absorption by anion-functionalized ionic liquids.

Journal of the American Chemical Society

Gurkan BE, de la Fuente JC, Mindrup EM, Ficke LE, Goodrich BF, Price EA, Schneider WF, Brennecke JF.
PMID: 20121150
J Am Chem Soc. 2010 Feb 24;132(7):2116-7. doi: 10.1021/ja909305t.

Amino acid ionic liquid trihexyl(tetradecyl)phosphonium methioninate [P(66614)][Met] and prolinate [P(66614)][Pro] absorb CO(2) in nearly 1:1 stoichiometry, surpassing by up to a factor of 2 the CO(2) capture efficiency of previously reported ionic liquid and aqueous amine absorbants for CO(2)....

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Gurkan BE, de la Fuente JC, Mindrup EM, et al. Equimolar CO(2) absorption by anion-functionalized ionic liquids. J Am Chem Soc. 2010;132(7):2116-7doi: 10.1021/ja909305t.
Gurkan, B. E., de la Fuente, J. C., Mindrup, E. M., Ficke, L. E., Goodrich, B. F., Price, E. A., Schneider, W. F., & Brennecke, J. F. (2010). Equimolar CO(2) absorption by anion-functionalized ionic liquids. Journal of the American Chemical Society, 132(7), 2116-7. https://doi.org/10.1021/ja909305t
Gurkan, Burcu E, et al. "Equimolar CO(2) absorption by anion-functionalized ionic liquids." Journal of the American Chemical Society vol. 132,7 (2010): 2116-7. doi: https://doi.org/10.1021/ja909305t
Gurkan BE, de la Fuente JC, Mindrup EM, Ficke LE, Goodrich BF, Price EA, Schneider WF, Brennecke JF. Equimolar CO(2) absorption by anion-functionalized ionic liquids. J Am Chem Soc. 2010 Feb 24;132(7):2116-7. doi: 10.1021/ja909305t. PMID: 20121150.
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Engineering solid-state morphologies in carbazole-ethynylene macrocycles.

Journal of the American Chemical Society

Finke AD, Gross DE, Han A, Moore JS.
PMID: 21774541
J Am Chem Soc. 2011 Sep 07;133(35):14063-70. doi: 10.1021/ja204795q. Epub 2011 Aug 11.

We present a crystallographic study that systematically investigates the effects of the n-alkyl side-chain length on the crystal packing in shape-persistent macrocycles. The solid-state packing of carbazole-ethynylene-containing macrocycles is sensitive to the alkyl-chain length. In macrocycles containing n-alkyl side...

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Finke AD, Gross DE, Han A, et al. Engineering solid-state morphologies in carbazole-ethynylene macrocycles. J Am Chem Soc. 2011;133(35):14063-70doi: 10.1021/ja204795q.
Finke, A. D., Gross, D. E., Han, A., & Moore, J. S. (2011). Engineering solid-state morphologies in carbazole-ethynylene macrocycles. Journal of the American Chemical Society, 133(35), 14063-70. https://doi.org/10.1021/ja204795q
Finke, Aaron D, et al. "Engineering solid-state morphologies in carbazole-ethynylene macrocycles." Journal of the American Chemical Society vol. 133,35 (2011): 14063-70. doi: https://doi.org/10.1021/ja204795q
Finke AD, Gross DE, Han A, Moore JS. Engineering solid-state morphologies in carbazole-ethynylene macrocycles. J Am Chem Soc. 2011 Sep 07;133(35):14063-70. doi: 10.1021/ja204795q. Epub 2011 Aug 11. PMID: 21774541.
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Supported-nanoparticle heterogeneous catalyst formation in contact with solution: kinetics and proposed mechanism for the conversion of Ir(1,5-COD)Cl/γ-Al2O3 to Ir(0)(~900)/γ-Al2O3.

Journal of the American Chemical Society

Mondloch JE, Finke RG.
PMID: 21526773
J Am Chem Soc. 2011 May 25;133(20):7744-56. doi: 10.1021/ja110550h. Epub 2011 Apr 28.

A current goal in heterogeneous catalysis is to transfer the synthetic, as well as developing mechanistic, insights from the modern revolution in nanoparticle science to the synthesis of supported-nanoparticle heterogeneous catalysts. In a recent study (Mondloch, J. E.; Wang,...

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Mondloch JE, Finke RG. Supported-nanoparticle heterogeneous catalyst formation in contact with solution: kinetics and proposed mechanism for the conversion of Ir(1,5-COD)Cl/γ-Al2O3 to Ir(0)(~900)/γ-Al2O3. J Am Chem Soc. 2011;133(20):7744-56doi: 10.1021/ja110550h.
Mondloch, J. E., & Finke, R. G. (2011). Supported-nanoparticle heterogeneous catalyst formation in contact with solution: kinetics and proposed mechanism for the conversion of Ir(1,5-COD)Cl/γ-Al2O3 to Ir(0)(~900)/γ-Al2O3. Journal of the American Chemical Society, 133(20), 7744-56. https://doi.org/10.1021/ja110550h
Mondloch, Joseph E, and Finke, Richard G. "Supported-nanoparticle heterogeneous catalyst formation in contact with solution: kinetics and proposed mechanism for the conversion of Ir(1,5-COD)Cl/γ-Al2O3 to Ir(0)(~900)/γ-Al2O3." Journal of the American Chemical Society vol. 133,20 (2011): 7744-56. doi: https://doi.org/10.1021/ja110550h
Mondloch JE, Finke RG. Supported-nanoparticle heterogeneous catalyst formation in contact with solution: kinetics and proposed mechanism for the conversion of Ir(1,5-COD)Cl/γ-Al2O3 to Ir(0)(~900)/γ-Al2O3. J Am Chem Soc. 2011 May 25;133(20):7744-56. doi: 10.1021/ja110550h. Epub 2011 Apr 28. PMID: 21526773.
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Showing 13 to 24 of 258 entries