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Substrate-induced variations of molecular packing, dynamics, and intermolecular electronic couplings in pentacene monolayers on the amorphous silica dielectric.

ACS nano

Viani L, Risko C, Toney MF, Breiby DW, Brédas JL.
PMID: 24369713
ACS Nano. 2014 Jan 28;8(1):690-700. doi: 10.1021/nn405399n. Epub 2014 Jan 06.

Charge-carrier transport in thin-film organic field-effect transistors takes place within the first (few) molecular layer(s) of the active organic material in contact with the gate dielectric. Here, we use atomistic molecular dynamics simulations to evaluate how interactions with bare...

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Viani L, Risko C, Toney MF, et al. Substrate-induced variations of molecular packing, dynamics, and intermolecular electronic couplings in pentacene monolayers on the amorphous silica dielectric. ACS Nano. 2014;8(1):690-700doi: 10.1021/nn405399n.
Viani, L., Risko, C., Toney, M. F., Breiby, D. W., & Brédas, J. L. (2014). Substrate-induced variations of molecular packing, dynamics, and intermolecular electronic couplings in pentacene monolayers on the amorphous silica dielectric. ACS nano, 8(1), 690-700. https://doi.org/10.1021/nn405399n
Viani, Lucas, et al. "Substrate-induced variations of molecular packing, dynamics, and intermolecular electronic couplings in pentacene monolayers on the amorphous silica dielectric." ACS nano vol. 8,1 (2014): 690-700. doi: https://doi.org/10.1021/nn405399n
Viani L, Risko C, Toney MF, Breiby DW, Brédas JL. Substrate-induced variations of molecular packing, dynamics, and intermolecular electronic couplings in pentacene monolayers on the amorphous silica dielectric. ACS Nano. 2014 Jan 28;8(1):690-700. doi: 10.1021/nn405399n. Epub 2014 Jan 06. PMID: 24369713.
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Beyond the Hammett Effect: Using Strain to Alter the Landscape of Electrochemical Potentials.

Chemphyschem : a European journal of chemical physics and physical chemistry

Casselman MD, Elliott CF, Modekrutti S, Zhang PL, Parkin SR, Risko C, Odom SA.
PMID: 28590586
Chemphyschem. 2017 Aug 18;18(16):2142-2146. doi: 10.1002/cphc.201700607. Epub 2017 Jun 21.

The substitution of sterically bulky groups at precise locations along the periphery of fused-ring aromatic systems is demonstrated to increase electrochemical oxidation potentials by preventing relaxation events in the oxidized state. Phenothiazines, which undergo significant geometric relaxation upon oxidation,...

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Casselman MD, Elliott CF, Modekrutti S, et al. Beyond the Hammett Effect: Using Strain to Alter the Landscape of Electrochemical Potentials. Chemphyschem. 2017;18(16):2142-2146doi: 10.1002/cphc.201700607.
Casselman, M. D., Elliott, C. F., Modekrutti, S., Zhang, P. L., Parkin, S. R., Risko, C., & Odom, S. A. (2017). Beyond the Hammett Effect: Using Strain to Alter the Landscape of Electrochemical Potentials. Chemphyschem : a European journal of chemical physics and physical chemistry, 18(16), 2142-2146. https://doi.org/10.1002/cphc.201700607
Casselman, Matthew D, et al. "Beyond the Hammett Effect: Using Strain to Alter the Landscape of Electrochemical Potentials." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 18,16 (2017): 2142-2146. doi: https://doi.org/10.1002/cphc.201700607
Casselman MD, Elliott CF, Modekrutti S, Zhang PL, Parkin SR, Risko C, Odom SA. Beyond the Hammett Effect: Using Strain to Alter the Landscape of Electrochemical Potentials. Chemphyschem. 2017 Aug 18;18(16):2142-2146. doi: 10.1002/cphc.201700607. Epub 2017 Jun 21. PMID: 28590586.
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N-substituted phenothiazine derivatives: how the stability of the neutral and radical cation forms affects overcharge performance in lithium-ion batteries.

Chemphyschem : a European journal of chemical physics and physical chemistry

Narayana KA, Casselman MD, Elliott CF, Ergun S, Parkin SR, Risko C, Odom SA.
PMID: 25504135
Chemphyschem. 2015 Apr 27;16(6):1179-89. doi: 10.1002/cphc.201402674. Epub 2014 Dec 11.

Phenothiazine and five N-substituted derivatives were evaluated as electrolyte additives for overcharge protection in LiFePO4 /synthetic graphite lithium-ion batteries. We report on the stability and reactivity of both the neutral and radical-cation forms of these six compounds. While three...

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Narayana KA, Casselman MD, Elliott CF, et al. N-substituted phenothiazine derivatives: how the stability of the neutral and radical cation forms affects overcharge performance in lithium-ion batteries. Chemphyschem. 2014;16(6):1179-89doi: 10.1002/cphc.201402674.
Narayana, K. A., Casselman, M. D., Elliott, C. F., Ergun, S., Parkin, S. R., Risko, C., & Odom, S. A. (2015). N-substituted phenothiazine derivatives: how the stability of the neutral and radical cation forms affects overcharge performance in lithium-ion batteries. Chemphyschem : a European journal of chemical physics and physical chemistry, 16(6), 1179-89. https://doi.org/10.1002/cphc.201402674
Narayana, Kishore Anand, et al. "N-substituted phenothiazine derivatives: how the stability of the neutral and radical cation forms affects overcharge performance in lithium-ion batteries." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 16,6 (2015): 1179-89. doi: https://doi.org/10.1002/cphc.201402674
Narayana KA, Casselman MD, Elliott CF, Ergun S, Parkin SR, Risko C, Odom SA. N-substituted phenothiazine derivatives: how the stability of the neutral and radical cation forms affects overcharge performance in lithium-ion batteries. Chemphyschem. 2015 Apr 27;16(6):1179-89. doi: 10.1002/cphc.201402674. Epub 2014 Dec 11. PMID: 25504135.
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n-Doping of organic electronic materials using air-stable organometallics: a mechanistic study of reduction by dimeric sandwich compounds.

Chemistry (Weinheim an der Bergstrasse, Germany)

Guo S, Mohapatra SK, Romanov A, Timofeeva TV, Hardcastle KI, Yesudas K, Risko C, Brédas JL, Marder SR, Barlow S.
PMID: 23108797
Chemistry. 2012 Nov 12;18(46):14760-72. doi: 10.1002/chem.201202591. Epub 2012 Oct 25.

Several 19-electron sandwich compounds are known to exist as "2×18-electron" dimers. Recently it has been shown that, despite their air stability in the solid state, some of these dimers act as powerful reductants when co-deposited from either the gas...

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Guo S, Mohapatra SK, Romanov A, et al. n-Doping of organic electronic materials using air-stable organometallics: a mechanistic study of reduction by dimeric sandwich compounds. Chemistry. 2012;18(46):14760-72doi: 10.1002/chem.201202591.
Guo, S., Mohapatra, S. K., Romanov, A., Timofeeva, T. V., Hardcastle, K. I., Yesudas, K., Risko, C., Brédas, J. L., Marder, S. R., & Barlow, S. (2012). n-Doping of organic electronic materials using air-stable organometallics: a mechanistic study of reduction by dimeric sandwich compounds. Chemistry (Weinheim an der Bergstrasse, Germany), 18(46), 14760-72. https://doi.org/10.1002/chem.201202591
Guo, Song, et al. "n-Doping of organic electronic materials using air-stable organometallics: a mechanistic study of reduction by dimeric sandwich compounds." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 18,46 (2012): 14760-72. doi: https://doi.org/10.1002/chem.201202591
Guo S, Mohapatra SK, Romanov A, Timofeeva TV, Hardcastle KI, Yesudas K, Risko C, Brédas JL, Marder SR, Barlow S. n-Doping of organic electronic materials using air-stable organometallics: a mechanistic study of reduction by dimeric sandwich compounds. Chemistry. 2012 Nov 12;18(46):14760-72. doi: 10.1002/chem.201202591. Epub 2012 Oct 25. PMID: 23108797.
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Impact of molecular packing on electronic polarization in organic crystals: the case of pentacene vs TIPS-pentacene.

Journal of the American Chemical Society

Ryno SM, Risko C, Brédas JL.
PMID: 24725006
J Am Chem Soc. 2014 Apr 30;136(17):6421-7. doi: 10.1021/ja501725s. Epub 2014 Apr 22.

Polarization energy corresponds to the stabilization of the cation or anion state of an atom or molecule when going from the gas phase to the solid state. The decrease in ionization energy and increase in electron affinity in the...

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Ryno SM, Risko C, Brédas JL. Impact of molecular packing on electronic polarization in organic crystals: the case of pentacene vs TIPS-pentacene. J Am Chem Soc. 2014;136(17):6421-7doi: 10.1021/ja501725s.
Ryno, S. M., Risko, C., & Brédas, J. L. (2014). Impact of molecular packing on electronic polarization in organic crystals: the case of pentacene vs TIPS-pentacene. Journal of the American Chemical Society, 136(17), 6421-7. https://doi.org/10.1021/ja501725s
Ryno, Sean M, et al. "Impact of molecular packing on electronic polarization in organic crystals: the case of pentacene vs TIPS-pentacene." Journal of the American Chemical Society vol. 136,17 (2014): 6421-7. doi: https://doi.org/10.1021/ja501725s
Ryno SM, Risko C, Brédas JL. Impact of molecular packing on electronic polarization in organic crystals: the case of pentacene vs TIPS-pentacene. J Am Chem Soc. 2014 Apr 30;136(17):6421-7. doi: 10.1021/ja501725s. Epub 2014 Apr 22. PMID: 24725006.
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Air-Stable Anisotropic Monocrystalline Nickel Nanowires Characterized Using Electron Holography.

Nano letters

Drisko GL, Gatel C, Fazzini PF, Ibarra A, Mourdikoudis S, Bley V, Fajerwerg K, Fau P, Kahn M.
PMID: 29406737
Nano Lett. 2018 Mar 14;18(3):1733-1738. doi: 10.1021/acs.nanolett.7b04791. Epub 2018 Feb 13.

Nickel is capable of discharging electric and magnetic shocks in aerospace materials thanks to its conductivity and magnetism. Nickel nanowires are especially desirable for such an application as electronic percolation can be achieved without significantly increasing the weight of...

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Drisko GL, Gatel C, Fazzini PF, et al. Air-Stable Anisotropic Monocrystalline Nickel Nanowires Characterized Using Electron Holography. Nano Lett. 2018;18(3):1733-1738doi: 10.1021/acs.nanolett.7b04791.
Drisko, G. L., Gatel, C., Fazzini, P. F., Ibarra, A., Mourdikoudis, S., Bley, V., Fajerwerg, K., Fau, P., & Kahn, M. (2018). Air-Stable Anisotropic Monocrystalline Nickel Nanowires Characterized Using Electron Holography. Nano letters, 18(3), 1733-1738. https://doi.org/10.1021/acs.nanolett.7b04791
Drisko, Glenna L, et al. "Air-Stable Anisotropic Monocrystalline Nickel Nanowires Characterized Using Electron Holography." Nano letters vol. 18,3 (2018): 1733-1738. doi: https://doi.org/10.1021/acs.nanolett.7b04791
Drisko GL, Gatel C, Fazzini PF, Ibarra A, Mourdikoudis S, Bley V, Fajerwerg K, Fau P, Kahn M. Air-Stable Anisotropic Monocrystalline Nickel Nanowires Characterized Using Electron Holography. Nano Lett. 2018 Mar 14;18(3):1733-1738. doi: 10.1021/acs.nanolett.7b04791. Epub 2018 Feb 13. PMID: 29406737.
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Computationally aided design of a high-performance organic semiconductor: the development of a universal crystal engineering core.

Chemical science

Petty AJ, Ai Q, Sorli JC, Haneef HF, Purdum GE, Boehm A, Granger DB, Gu K, Rubinger CPL, Parkin SR, Graham KR, Jurchescu OD, Loo YL, Risko C, Anthony JE.
PMID: 32055377
Chem Sci. 2019 Oct 07;10(45):10543-10549. doi: 10.1039/c9sc02930c. eCollection 2019 Dec 07.

Herein, we describe the design and synthesis of a suite of molecules based on a benzodithiophene "universal crystal engineering core". After computationally screening derivatives, a trialkylsilylethyne-based crystal engineering strategy was employed to tailor the crystal packing for use as...

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Petty AJ, Ai Q, Sorli JC, et al. Computationally aided design of a high-performance organic semiconductor: the development of a universal crystal engineering core. Chem Sci. 2019;10(45):10543-10549doi: 10.1039/c9sc02930c.
Petty, A. J., Ai, Q., Sorli, J. C., Haneef, H. F., Purdum, G. E., Boehm, A., Granger, D. B., Gu, K., Rubinger, C. P. L., Parkin, S. R., Graham, K. R., Jurchescu, O. D., Loo, Y. L., Risko, C., & Anthony, J. E. (2019). Computationally aided design of a high-performance organic semiconductor: the development of a universal crystal engineering core. Chemical science, 10(45), 10543-10549. https://doi.org/10.1039/c9sc02930c
Petty, Anthony J, et al. "Computationally aided design of a high-performance organic semiconductor: the development of a universal crystal engineering core." Chemical science vol. 10,45 (2019): 10543-10549. doi: https://doi.org/10.1039/c9sc02930c
Petty AJ, Ai Q, Sorli JC, Haneef HF, Purdum GE, Boehm A, Granger DB, Gu K, Rubinger CPL, Parkin SR, Graham KR, Jurchescu OD, Loo YL, Risko C, Anthony JE. Computationally aided design of a high-performance organic semiconductor: the development of a universal crystal engineering core. Chem Sci. 2019 Oct 07;10(45):10543-10549. doi: 10.1039/c9sc02930c. eCollection 2019 Dec 07. PMID: 32055377; PMCID: PMC6988752.
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Synthesis, characterization, and transistor response of semiconducting silole polymers with substantial hole mobility and air stability. Experiment and theory.

Journal of the American Chemical Society

Lu G, Usta H, Risko C, Wang L, Facchetti A, Ratner MA, Marks TJ.
PMID: 18505257
J Am Chem Soc. 2008 Jun 18;130(24):7670-85. doi: 10.1021/ja800424m. Epub 2008 May 28.

Realizing p-channel semiconducting polymers with good hole mobility, solution processibility, and air stability is an important step forward in the chemical manipulation of charge transport in polymeric solids and in the development of low-cost printed electronics. We report here...

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Lu G, Usta H, Risko C, et al. Synthesis, characterization, and transistor response of semiconducting silole polymers with substantial hole mobility and air stability. Experiment and theory. J Am Chem Soc. 2008;130(24):7670-85doi: 10.1021/ja800424m.
Lu, G., Usta, H., Risko, C., Wang, L., Facchetti, A., Ratner, M. A., & Marks, T. J. (2008). Synthesis, characterization, and transistor response of semiconducting silole polymers with substantial hole mobility and air stability. Experiment and theory. Journal of the American Chemical Society, 130(24), 7670-85. https://doi.org/10.1021/ja800424m
Lu, Gang, et al. "Synthesis, characterization, and transistor response of semiconducting silole polymers with substantial hole mobility and air stability. Experiment and theory." Journal of the American Chemical Society vol. 130,24 (2008): 7670-85. doi: https://doi.org/10.1021/ja800424m
Lu G, Usta H, Risko C, Wang L, Facchetti A, Ratner MA, Marks TJ. Synthesis, characterization, and transistor response of semiconducting silole polymers with substantial hole mobility and air stability. Experiment and theory. J Am Chem Soc. 2008 Jun 18;130(24):7670-85. doi: 10.1021/ja800424m. Epub 2008 May 28. PMID: 18505257.
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Double-Sided Electrochromic Device Based on Metal-Organic Frameworks.

ACS applied materials & interfaces

Mjejri I, Doherty CM, Rubio-Martinez M, Drisko GL, Rougier A.
PMID: 29043775
ACS Appl Mater Interfaces. 2017 Nov 22;9(46):39930-39934. doi: 10.1021/acsami.7b13647. Epub 2017 Nov 08.

Devices displaying controllably tunable optical properties through an applied voltage are attractive for smart glass, mirrors, and displays. Electrochromic material development aims to decrease power consumption while increasing the variety of attainable colors, their brilliance, and their longevity. We...

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Mjejri I, Doherty CM, Rubio-Martinez M, et al. Double-Sided Electrochromic Device Based on Metal-Organic Frameworks. ACS Appl Mater Interfaces. 2017;9(46):39930-39934doi: 10.1021/acsami.7b13647.
Mjejri, I., Doherty, C. M., Rubio-Martinez, M., Drisko, G. L., & Rougier, A. (2017). Double-Sided Electrochromic Device Based on Metal-Organic Frameworks. ACS applied materials & interfaces, 9(46), 39930-39934. https://doi.org/10.1021/acsami.7b13647
Mjejri, Issam, et al. "Double-Sided Electrochromic Device Based on Metal-Organic Frameworks." ACS applied materials & interfaces vol. 9,46 (2017): 39930-39934. doi: https://doi.org/10.1021/acsami.7b13647
Mjejri I, Doherty CM, Rubio-Martinez M, Drisko GL, Rougier A. Double-Sided Electrochromic Device Based on Metal-Organic Frameworks. ACS Appl Mater Interfaces. 2017 Nov 22;9(46):39930-39934. doi: 10.1021/acsami.7b13647. Epub 2017 Nov 08. PMID: 29043775.
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Presence of Short Intermolecular Contacts Screens for Kinetic Stability in Packing Polymorphs.

Journal of the American Chemical Society

Purdum GE, Telesz NG, Jarolimek K, Ryno SM, Gessner T, Davy NC, Petty AJ, Zhen Y, Shu Y, Facchetti A, Collis GE, Hu W, Wu C, Anthony JE, Weitz RT, Risko C, Loo YL.
PMID: 29793338
J Am Chem Soc. 2018 Jun 20;140(24):7519-7525. doi: 10.1021/jacs.8b01421. Epub 2018 Jun 08.

Polymorphism is pervasive in molecular solids. While computational predictions of the molecular polymorphic landscape have improved significantly, identifying which polymorphs are preferentially accessed and experimentally stable remains a challenge. We report a framework that correlates short intermolecular contacts with...

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Purdum GE, Telesz NG, Jarolimek K, et al. Presence of Short Intermolecular Contacts Screens for Kinetic Stability in Packing Polymorphs. J Am Chem Soc. 2018;140(24):7519-7525doi: 10.1021/jacs.8b01421.
Purdum, G. E., Telesz, N. G., Jarolimek, K., Ryno, S. M., Gessner, T., Davy, N. C., Petty, A. J., Zhen, Y., Shu, Y., Facchetti, A., Collis, G. E., Hu, W., Wu, C., Anthony, J. E., Weitz, R. T., Risko, C., & Loo, Y. L. (2018). Presence of Short Intermolecular Contacts Screens for Kinetic Stability in Packing Polymorphs. Journal of the American Chemical Society, 140(24), 7519-7525. https://doi.org/10.1021/jacs.8b01421
Purdum, Geoffrey E, et al. "Presence of Short Intermolecular Contacts Screens for Kinetic Stability in Packing Polymorphs." Journal of the American Chemical Society vol. 140,24 (2018): 7519-7525. doi: https://doi.org/10.1021/jacs.8b01421
Purdum GE, Telesz NG, Jarolimek K, Ryno SM, Gessner T, Davy NC, Petty AJ, Zhen Y, Shu Y, Facchetti A, Collis GE, Hu W, Wu C, Anthony JE, Weitz RT, Risko C, Loo YL. Presence of Short Intermolecular Contacts Screens for Kinetic Stability in Packing Polymorphs. J Am Chem Soc. 2018 Jun 20;140(24):7519-7525. doi: 10.1021/jacs.8b01421. Epub 2018 Jun 08. PMID: 29793338.
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On describing the optoelectronic characteristics of poly(benzodithiophene-co-quinoxaline)-fullerene complexes: the influence of optimally tuned density functionals.

Physical chemistry chemical physics : PCCP

Kastinen T, Niskanen M, Risko C, Cramariuc O, Hukka TI.
PMID: 27722580
Phys Chem Chem Phys. 2016 Oct 05;18(39):27654-27670. doi: 10.1039/c6cp04567g.

Here, we investigate the effects of both tuning the range-separation parameter of long-range corrected (LRC) density functionals and including dispersion corrections on describing the local optoelectronic properties of polymer-fullerene interfaces that are critical to the performance of polymer solar...

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Kastinen T, Niskanen M, Risko C, et al. On describing the optoelectronic characteristics of poly(benzodithiophene-co-quinoxaline)-fullerene complexes: the influence of optimally tuned density functionals. Phys Chem Chem Phys. 2016;18(39):27654-27670doi: 10.1039/c6cp04567g.
Kastinen, T., Niskanen, M., Risko, C., Cramariuc, O., & Hukka, T. I. (2016). On describing the optoelectronic characteristics of poly(benzodithiophene-co-quinoxaline)-fullerene complexes: the influence of optimally tuned density functionals. Physical chemistry chemical physics : PCCP, 18(39), 27654-27670. https://doi.org/10.1039/c6cp04567g
Kastinen, T, et al. "On describing the optoelectronic characteristics of poly(benzodithiophene-co-quinoxaline)-fullerene complexes: the influence of optimally tuned density functionals." Physical chemistry chemical physics : PCCP vol. 18,39 (2016): 27654-27670. doi: https://doi.org/10.1039/c6cp04567g
Kastinen T, Niskanen M, Risko C, Cramariuc O, Hukka TI. On describing the optoelectronic characteristics of poly(benzodithiophene-co-quinoxaline)-fullerene complexes: the influence of optimally tuned density functionals. Phys Chem Chem Phys. 2016 Oct 05;18(39):27654-27670. doi: 10.1039/c6cp04567g. PMID: 27722580.
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"Natural" isomolecular hormone replacement: an evidence-based medicine approach.

International journal of pharmaceutical compounding

Drisko JA.
PMID: 23981731
Int J Pharm Compd. 2000 Nov-Dec;4(6):414-20.

No abstract available.

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Drisko JA. "Natural" isomolecular hormone replacement: an evidence-based medicine approach. Int J Pharm Compd. 2000;4(6):414-20
Drisko, J. A. (2000). "Natural" isomolecular hormone replacement: an evidence-based medicine approach. International journal of pharmaceutical compounding, 4(6), 414-20.
Drisko, J A. ""Natural" isomolecular hormone replacement: an evidence-based medicine approach." International journal of pharmaceutical compounding vol. 4,6 (2000): 414-20.
Drisko JA. "Natural" isomolecular hormone replacement: an evidence-based medicine approach. Int J Pharm Compd. 2000 Nov-Dec;4(6):414-20. PMID: 23981731.
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Showing 1 to 12 of 86 entries