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Showing 1 to 12 of 235 entries
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Stabilizing Pentacene By Cyclopentannulation.

Angewandte Chemie (International ed. in English)

Bheemireddy SR, Ubaldo PC, Rose PW, Finke AD, Zhuang J, Wang L, Plunkett KN.
PMID: 26768696
Angew Chem Int Ed Engl. 2015 Dec 21;54(52):15762-6. doi: 10.1002/anie.201508650. Epub 2015 Nov 19.

A new class of stabilized pentacene derivatives with externally fused five-membered rings are prepared by means of a key palladium-catalyzed cyclopentannulation step. The target compounds are synthesized by chemical manipulation of a partially saturated 6,13-dibromopentacene precursor that can be...

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Bheemireddy SR, Ubaldo PC, Rose PW, et al. Stabilizing Pentacene By Cyclopentannulation. Angew Chem Int Ed Engl. 2015;54(52):15762-6doi: 10.1002/anie.201508650.
Bheemireddy, S. R., Ubaldo, P. C., Rose, P. W., Finke, A. D., Zhuang, J., Wang, L., & Plunkett, K. N. (2015). Stabilizing Pentacene By Cyclopentannulation. Angewandte Chemie (International ed. in English), 54(52), 15762-6. https://doi.org/10.1002/anie.201508650
Bheemireddy, Sambasiva R, et al. "Stabilizing Pentacene By Cyclopentannulation." Angewandte Chemie (International ed. in English) vol. 54,52 (2015): 15762-6. doi: https://doi.org/10.1002/anie.201508650
Bheemireddy SR, Ubaldo PC, Rose PW, Finke AD, Zhuang J, Wang L, Plunkett KN. Stabilizing Pentacene By Cyclopentannulation. Angew Chem Int Ed Engl. 2015 Dec 21;54(52):15762-6. doi: 10.1002/anie.201508650. Epub 2015 Nov 19. PMID: 26768696.
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Crystal structures of three complexes of zinc chloride with tri-tert-butyl-phosphane.

Acta crystallographica. Section E, Crystallographic communications

Finke AD, Gray DL, Moore JS.
PMID: 26870580
Acta Crystallogr E Crystallogr Commun. 2016 Jan 01;72:35-9. doi: 10.1107/S2056989015023373. eCollection 2016 Jan 01.

Under anhydrous conditions and in the absence of a Lewis-base solvent, a zinc chloride complex with tri-tert-butyl-phosphane as the μ-bridged dimer is formed, viz. di-μ-chlorido-bis-[chlorido-bis-(tri-tert-butyl-phosphane)zinc], [ZnCl4(C12H27P)2], (1), which features a nearly square-shaped (ZnCl)2 cyclic core and whose Cl atoms...

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Finke AD, Gray DL, Moore JS. Crystal structures of three complexes of zinc chloride with tri-tert-butyl-phosphane. Acta Crystallogr E Crystallogr Commun. 2016;72:35-9doi: 10.1107/S2056989015023373.
Finke, A. D., Gray, D. L., & Moore, J. S. (2016). Crystal structures of three complexes of zinc chloride with tri-tert-butyl-phosphane. Acta crystallographica. Section E, Crystallographic communications, 7235-9. https://doi.org/10.1107/S2056989015023373
Finke, Aaron D, et al. "Crystal structures of three complexes of zinc chloride with tri-tert-butyl-phosphane." Acta crystallographica. Section E, Crystallographic communications vol. 72 (2016): 35-9. doi: https://doi.org/10.1107/S2056989015023373
Finke AD, Gray DL, Moore JS. Crystal structures of three complexes of zinc chloride with tri-tert-butyl-phosphane. Acta Crystallogr E Crystallogr Commun. 2016 Jan 01;72:35-9. doi: 10.1107/S2056989015023373. eCollection 2016 Jan 01. PMID: 26870580; PMCID: PMC4704762.
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Pentaindenocorannulene: Properties, Assemblies, and C.

Angewandte Chemie (International ed. in English)

Lampart S, Roch LM, Dutta AK, Wang Y, Warshamanage R, Finke AD, Linden A, Baldridge KK, Siegel JS.
PMID: 27709796
Angew Chem Int Ed Engl. 2016 Nov 14;55(47):14648-14652. doi: 10.1002/anie.201608337. Epub 2016 Oct 06.

Pentaindenocorannulene (C

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Lampart S, Roch LM, Dutta AK, et al. Pentaindenocorannulene: Properties, Assemblies, and C. Angew Chem Int Ed Engl. 2016;55(47):14648-14652doi: 10.1002/anie.201608337.
Lampart, S., Roch, L. M., Dutta, A. K., Wang, Y., Warshamanage, R., Finke, A. D., Linden, A., Baldridge, K. K., & Siegel, J. S. (2016). Pentaindenocorannulene: Properties, Assemblies, and C. Angewandte Chemie (International ed. in English), 55(47), 14648-14652. https://doi.org/10.1002/anie.201608337
Lampart, Samuel, et al. "Pentaindenocorannulene: Properties, Assemblies, and C." Angewandte Chemie (International ed. in English) vol. 55,47 (2016): 14648-14652. doi: https://doi.org/10.1002/anie.201608337
Lampart S, Roch LM, Dutta AK, Wang Y, Warshamanage R, Finke AD, Linden A, Baldridge KK, Siegel JS. Pentaindenocorannulene: Properties, Assemblies, and C. Angew Chem Int Ed Engl. 2016 Nov 14;55(47):14648-14652. doi: 10.1002/anie.201608337. Epub 2016 Oct 06. PMID: 27709796.
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Friendship: Operationalizing the Intangible to Improve Friendship-Based Outcomes for Individuals With Autism Spectrum Disorder.

American journal of speech-language pathology

Finke EH.
PMID: 27716859
Am J Speech Lang Pathol. 2016 Nov 01;25(4):654-663. doi: 10.1044/2016_AJSLP-15-0042.

PURPOSE: Individuals with autism spectrum disorder (ASD) have social deficits that affect making and maintaining friends. Many empirically tested methods to address these social deficits are available, yet difficulties related to the establishment and maintenance of authentic friendships persist.METHOD:...

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Finke EH. Friendship: Operationalizing the Intangible to Improve Friendship-Based Outcomes for Individuals With Autism Spectrum Disorder. Am J Speech Lang Pathol. 2016;25(4):654-663doi: 10.1044/2016_AJSLP-15-0042.
Finke, E. H. (2016). Friendship: Operationalizing the Intangible to Improve Friendship-Based Outcomes for Individuals With Autism Spectrum Disorder. American journal of speech-language pathology, 25(4), 654-663. https://doi.org/10.1044/2016_AJSLP-15-0042
Finke, Erinn H. "Friendship: Operationalizing the Intangible to Improve Friendship-Based Outcomes for Individuals With Autism Spectrum Disorder." American journal of speech-language pathology vol. 25,4 (2016): 654-663. doi: https://doi.org/10.1044/2016_AJSLP-15-0042
Finke EH. Friendship: Operationalizing the Intangible to Improve Friendship-Based Outcomes for Individuals With Autism Spectrum Disorder. Am J Speech Lang Pathol. 2016 Nov 01;25(4):654-663. doi: 10.1044/2016_AJSLP-15-0042. PMID: 27716859.
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Soliciting feedback: on becoming an effective clinical teacher.

Journal of general internal medicine

Orlander JD, Fincke BG.
PMID: 8077998
J Gen Intern Med. 1994 Jun;9(6):334-5. doi: 10.1007/BF02599182.

The art of teaching is difficult to master. When teaching in small groups, as often happens in clinical medicine, there is an opportunity to find out what works by speaking directly with students. The information they provide can serve...

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Orlander JD, Fincke BG. Soliciting feedback: on becoming an effective clinical teacher. J Gen Intern Med. 1994;9(6):334-5doi: 10.1007/BF02599182.
Orlander, J. D., & Fincke, B. G. (1994). Soliciting feedback: on becoming an effective clinical teacher. Journal of general internal medicine, 9(6), 334-5. https://doi.org/10.1007/BF02599182
Orlander, J D, and Fincke, B G. "Soliciting feedback: on becoming an effective clinical teacher." Journal of general internal medicine vol. 9,6 (1994): 334-5. doi: https://doi.org/10.1007/BF02599182
Orlander JD, Fincke BG. Soliciting feedback: on becoming an effective clinical teacher. J Gen Intern Med. 1994 Jun;9(6):334-5. doi: 10.1007/BF02599182. PMID: 8077998.
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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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Early local last glacial maximum in the tropical Andes.

Science (New York, N.Y.)

Smith JA, Seltzer GO, Farber DL, Rodbell DT, Finkel RC.
PMID: 15860623
Science. 2005 Apr 29;308(5722):678-81. doi: 10.1126/science.1107075.

The local last glacial maximum in the tropical Andes was earlier and less extensive than previously thought, based on 106 cosmogenic ages (from beryllium-10 dating) from moraines in Peru and Bolivia. Glaciers reached their greatest extent in the last...

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Smith JA, Seltzer GO, Farber DL, et al. Early local last glacial maximum in the tropical Andes. Science. 2005;308(5722):678-81doi: 10.1126/science.1107075.
Smith, J. A., Seltzer, G. O., Farber, D. L., Rodbell, D. T., & Finkel, R. C. (2005). Early local last glacial maximum in the tropical Andes. Science (New York, N.Y.), 308(5722), 678-81. https://doi.org/10.1126/science.1107075
Smith, Jacqueline A, et al. "Early local last glacial maximum in the tropical Andes." Science (New York, N.Y.) vol. 308,5722 (2005): 678-81. doi: https://doi.org/10.1126/science.1107075
Smith JA, Seltzer GO, Farber DL, Rodbell DT, Finkel RC. Early local last glacial maximum in the tropical Andes. Science. 2005 Apr 29;308(5722):678-81. doi: 10.1126/science.1107075. PMID: 15860623.
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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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Pattern of bombardment-produced radionuclides in rock 10017 and in lunar soil.

Science (New York, N.Y.)

Shedlovsky JP, Honda M, Reedy RC, Evans JC, Lal D, Lindstrom RM, Delany AC, Arnold JR, Loosli HH, Fruchter JS, Finkel RC.
PMID: 17781502
Science. 1970 Jan 30;167(3918):574-6. doi: 10.1126/science.167.3918.574.

A large number of radionuclides have been measured as a function of depth in lunar rock 10017 and in bulk fines. Data are reported on (10)Be, (22)Na, (26)Al, (36)Cl, (49)V, (53)mn, (54)Mn (55)Fe, (56)Co, (57)Co, and (59)Ni and on...

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Shedlovsky JP, Honda M, Reedy RC, et al. Pattern of bombardment-produced radionuclides in rock 10017 and in lunar soil. Science. 1970;167(3918):574-6doi: 10.1126/science.167.3918.574.
Shedlovsky, J. P., Honda, M., Reedy, R. C., Evans, J. C., Lal, D., Lindstrom, R. M., Delany, A. C., Arnold, J. R., Loosli, H. H., Fruchter, J. S., & Finkel, R. C. (1970). Pattern of bombardment-produced radionuclides in rock 10017 and in lunar soil. Science (New York, N.Y.), 167(3918), 574-6. https://doi.org/10.1126/science.167.3918.574
Shedlovsky, J P, et al. "Pattern of bombardment-produced radionuclides in rock 10017 and in lunar soil." Science (New York, N.Y.) vol. 167,3918 (1970): 574-6. doi: https://doi.org/10.1126/science.167.3918.574
Shedlovsky JP, Honda M, Reedy RC, Evans JC, Lal D, Lindstrom RM, Delany AC, Arnold JR, Loosli HH, Fruchter JS, Finkel RC. Pattern of bombardment-produced radionuclides in rock 10017 and in lunar soil. Science. 1970 Jan 30;167(3918):574-6. doi: 10.1126/science.167.3918.574. PMID: 17781502.
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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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Adhesion of microcapsules.

Langmuir : the ACS journal of surfaces and colloids

Graf P, Finken R, Seifert U.
PMID: 16893199
Langmuir. 2006 Aug 15;22(17):7117-9. doi: 10.1021/la060803l.

The adhesion of microcapsules to an attractive contact potential is studied theoretically. The axisymmetric shape equations are solved numerically. Beyond a universal threshold strength of the potential, the contact radius increases in proportion to the square root of the...

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Graf P, Finken R, Seifert U. Adhesion of microcapsules. Langmuir. 2006;22(17):7117-9doi: 10.1021/la060803l.
Graf, P., Finken, R., & Seifert, U. (2006). Adhesion of microcapsules. Langmuir : the ACS journal of surfaces and colloids, 22(17), 7117-9. https://doi.org/10.1021/la060803l
Graf, Peter, et al. "Adhesion of microcapsules." Langmuir : the ACS journal of surfaces and colloids vol. 22,17 (2006): 7117-9. doi: https://doi.org/10.1021/la060803l
Graf P, Finken R, Seifert U. Adhesion of microcapsules. Langmuir. 2006 Aug 15;22(17):7117-9. doi: 10.1021/la060803l. PMID: 16893199.
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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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Showing 1 to 12 of 235 entries