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Hybrid 3D Printing of Soft Electronics.

Advanced materials (Deerfield Beach, Fla.)

Valentine AD, Busbee TA, Boley JW, Raney JR, Chortos A, Kotikian A, Berrigan JD, Durstock MF, Lewis JA.
PMID: 28875572
Adv Mater. 2017 Oct;29(40). doi: 10.1002/adma.201703817. Epub 2017 Sep 06.

Hybrid 3D printing is a new method for producing soft electronics that combines direct ink writing of conductive and dielectric elastomeric materials with automated pick-and-place of surface mount electronic components within an integrated additive manufacturing platform. Using this approach,...

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Valentine AD, Busbee TA, Boley JW, et al. Hybrid 3D Printing of Soft Electronics. Adv Mater. 2017;29(40)doi: 10.1002/adma.201703817.
Valentine, A. D., Busbee, T. A., Boley, J. W., Raney, J. R., Chortos, A., Kotikian, A., Berrigan, J. D., Durstock, M. F., & Lewis, J. A. (2017). Hybrid 3D Printing of Soft Electronics. Advanced materials (Deerfield Beach, Fla.), 29(40), . https://doi.org/10.1002/adma.201703817
Valentine, Alexander D, et al. "Hybrid 3D Printing of Soft Electronics." Advanced materials (Deerfield Beach, Fla.) vol. 29,40 (2017). doi: https://doi.org/10.1002/adma.201703817
Valentine AD, Busbee TA, Boley JW, Raney JR, Chortos A, Kotikian A, Berrigan JD, Durstock MF, Lewis JA. Hybrid 3D Printing of Soft Electronics. Adv Mater. 2017 Oct;29(40). doi: 10.1002/adma.201703817. Epub 2017 Sep 06. PMID: 28875572.
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Shape of Multireference, Equation-of-Motion Coupled-Cluster, and Density Functional Theory Potential Energy Surfaces at a Conical Intersection.

Journal of chemical theory and computation

Gozem S, Melaccio F, Valentini A, Filatov M, Huix-Rotllant M, Ferré N, Frutos LM, Angeli C, Krylov AI, Granovsky AA, Lindh R, Olivucci M.
PMID: 26588278
J Chem Theory Comput. 2014 Aug 12;10(8):3074-84. doi: 10.1021/ct500154k. Epub 2014 Jun 11.

We report and characterize ground-state and excited-state potential energy profiles using a variety of electronic structure methods along a loop lying on the branching plane associated with a conical intersection (CI) of a reduced retinal model, the penta-2,4-dieniminium cation...

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Gozem S, Melaccio F, Valentini A, et al. Shape of Multireference, Equation-of-Motion Coupled-Cluster, and Density Functional Theory Potential Energy Surfaces at a Conical Intersection. J Chem Theory Comput. 2014;10(8):3074-84doi: 10.1021/ct500154k.
Gozem, S., Melaccio, F., Valentini, A., Filatov, M., Huix-Rotllant, M., Ferré, N., Frutos, L. M., Angeli, C., Krylov, A. I., Granovsky, A. A., Lindh, R., & Olivucci, M. (2014). Shape of Multireference, Equation-of-Motion Coupled-Cluster, and Density Functional Theory Potential Energy Surfaces at a Conical Intersection. Journal of chemical theory and computation, 10(8), 3074-84. https://doi.org/10.1021/ct500154k
Gozem, Samer, et al. "Shape of Multireference, Equation-of-Motion Coupled-Cluster, and Density Functional Theory Potential Energy Surfaces at a Conical Intersection." Journal of chemical theory and computation vol. 10,8 (2014): 3074-84. doi: https://doi.org/10.1021/ct500154k
Gozem S, Melaccio F, Valentini A, Filatov M, Huix-Rotllant M, Ferré N, Frutos LM, Angeli C, Krylov AI, Granovsky AA, Lindh R, Olivucci M. Shape of Multireference, Equation-of-Motion Coupled-Cluster, and Density Functional Theory Potential Energy Surfaces at a Conical Intersection. J Chem Theory Comput. 2014 Aug 12;10(8):3074-84. doi: 10.1021/ct500154k. Epub 2014 Jun 11. PMID: 26588278.
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Direct Observation of Self-Organized Water-Containing Structures in the Liquid Phase and Their Influence on 5-(Hydroxymethyl)furfural Formation in Ionic Liquids.

Angewandte Chemie (International ed. in English)

Kashin AS, Galkin KI, Khokhlova EA, Ananikov VP.
PMID: 26754786
Angew Chem Int Ed Engl. 2016 Feb 05;55(6):2161-6. doi: 10.1002/anie.201510090. Epub 2016 Jan 11.

Water-containing organic solutions are widespread reaction media in organic synthesis and catalysis. This type of multicomponent liquid system has a number of unique properties because of the tendency for water to self-organize in mixtures with other liquids. The characterization...

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Kashin AS, Galkin KI, Khokhlova EA, et al. Direct Observation of Self-Organized Water-Containing Structures in the Liquid Phase and Their Influence on 5-(Hydroxymethyl)furfural Formation in Ionic Liquids. Angew Chem Int Ed Engl. 2016;55(6):2161-6doi: 10.1002/anie.201510090.
Kashin, A. S., Galkin, K. I., Khokhlova, E. A., & Ananikov, V. P. (2016). Direct Observation of Self-Organized Water-Containing Structures in the Liquid Phase and Their Influence on 5-(Hydroxymethyl)furfural Formation in Ionic Liquids. Angewandte Chemie (International ed. in English), 55(6), 2161-6. https://doi.org/10.1002/anie.201510090
Kashin, Alexey S, et al. "Direct Observation of Self-Organized Water-Containing Structures in the Liquid Phase and Their Influence on 5-(Hydroxymethyl)furfural Formation in Ionic Liquids." Angewandte Chemie (International ed. in English) vol. 55,6 (2016): 2161-6. doi: https://doi.org/10.1002/anie.201510090
Kashin AS, Galkin KI, Khokhlova EA, Ananikov VP. Direct Observation of Self-Organized Water-Containing Structures in the Liquid Phase and Their Influence on 5-(Hydroxymethyl)furfural Formation in Ionic Liquids. Angew Chem Int Ed Engl. 2016 Feb 05;55(6):2161-6. doi: 10.1002/anie.201510090. Epub 2016 Jan 11. PMID: 26754786.
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Modulating the electronic structure of chromophores by chemical substituents for efficient energy transfer: application to fluorone.

The journal of physical chemistry. A

Sand AM, Liu C, Valentine AJ, Mazziotti DA.
PMID: 25062094
J Phys Chem A. 2014 Aug 07;118(31):6085-91. doi: 10.1021/jp503900m. Epub 2014 Jul 25.

Strong electron correlation within a quasi-spin model of chromophores was recently shown to enhance exciton energy transfer significantly. Here we investigate how the modulation of the electronic structure of the chromophores by chemical substitution can enhance energy-transfer efficiency. Unlike...

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Sand AM, Liu C, Valentine AJ, et al. Modulating the electronic structure of chromophores by chemical substituents for efficient energy transfer: application to fluorone. J Phys Chem A. 2014;118(31):6085-91doi: 10.1021/jp503900m.
Sand, A. M., Liu, C., Valentine, A. J., & Mazziotti, D. A. (2014). Modulating the electronic structure of chromophores by chemical substituents for efficient energy transfer: application to fluorone. The journal of physical chemistry. A, 118(31), 6085-91. https://doi.org/10.1021/jp503900m
Sand, Andrew M, et al. "Modulating the electronic structure of chromophores by chemical substituents for efficient energy transfer: application to fluorone." The journal of physical chemistry. A vol. 118,31 (2014): 6085-91. doi: https://doi.org/10.1021/jp503900m
Sand AM, Liu C, Valentine AJ, Mazziotti DA. Modulating the electronic structure of chromophores by chemical substituents for efficient energy transfer: application to fluorone. J Phys Chem A. 2014 Aug 07;118(31):6085-91. doi: 10.1021/jp503900m. Epub 2014 Jul 25. PMID: 25062094.
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Polyfluorinated ethanes as versatile fluorinated C2-building blocks for organic synthesis.

Chemical reviews

Nenajdenko VG, Muzalevskiy VM, Shastin AV.
PMID: 25594605
Chem Rev. 2015 Jan 28;115(2):973-1050. doi: 10.1021/cr500465n. Epub 2015 Jan 16.

No abstract available.

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Nenajdenko VG, Muzalevskiy VM, Shastin AV. Polyfluorinated ethanes as versatile fluorinated C2-building blocks for organic synthesis. Chem Rev. 2015;115(2):973-1050doi: 10.1021/cr500465n.
Nenajdenko, V. G., Muzalevskiy, V. M., & Shastin, A. V. (2015). Polyfluorinated ethanes as versatile fluorinated C2-building blocks for organic synthesis. Chemical reviews, 115(2), 973-1050. https://doi.org/10.1021/cr500465n
Nenajdenko, Valentine G, et al. "Polyfluorinated ethanes as versatile fluorinated C2-building blocks for organic synthesis." Chemical reviews vol. 115,2 (2015): 973-1050. doi: https://doi.org/10.1021/cr500465n
Nenajdenko VG, Muzalevskiy VM, Shastin AV. Polyfluorinated ethanes as versatile fluorinated C2-building blocks for organic synthesis. Chem Rev. 2015 Jan 28;115(2):973-1050. doi: 10.1021/cr500465n. Epub 2015 Jan 16. PMID: 25594605.
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Antisymmetric Amino-Wagging Band of Hydrazine up to K' = 13 Levels.

Journal of molecular spectroscopy

Gulaczyk I, Kr M, Valentin A.
PMID: 9446763
J Mol Spectrosc. 1997 Dec;186(2):246-8. doi: 10.1006/jmsp.1997.7402.

A newly recorded high-resolution infrared spectrum of hydrazine has been studied in the 729-1198 cm-1 region (the nu12 antisymmetric wagging band) with a resolution of 0.002 cm-1. About 1350 transitions with K' from 7 to 13 have been newly...

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Gulaczyk I, Kr M, Valentin A. Antisymmetric Amino-Wagging Band of Hydrazine up to K' = 13 Levels. J Mol Spectrosc. 1997;186(2):246-8doi: 10.1006/jmsp.1997.7402.
Gulaczyk, I., Kr, M., & Valentin, A. (1997). Antisymmetric Amino-Wagging Band of Hydrazine up to K' = 13 Levels. Journal of molecular spectroscopy, 186(2), 246-8. https://doi.org/10.1006/jmsp.1997.7402
Gulaczyk, et al. "Antisymmetric Amino-Wagging Band of Hydrazine up to K' = 13 Levels." Journal of molecular spectroscopy vol. 186,2 (1997): 246-8. doi: https://doi.org/10.1006/jmsp.1997.7402
Gulaczyk I, Kr M, Valentin A. Antisymmetric Amino-Wagging Band of Hydrazine up to K' = 13 Levels. J Mol Spectrosc. 1997 Dec;186(2):246-8. doi: 10.1006/jmsp.1997.7402. PMID: 9446763.
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Novel efficient synthesis of dibromoalkenes. A first example of catalytic olefination of aliphatic carbonyl compounds.

Organic & biomolecular chemistry

Korotchenko VN, Shastin AV, Nenajdenko VG, Balenkova ES.
PMID: 12945772
Org Biomol Chem. 2003 Jun 07;1(11):1906-8. doi: 10.1039/b303221c.

A new simple and efficient one pot transformation of various aliphatic carbonyl compounds to the corresponding dibromoalkenes is described. A wide range of hydrazones of aldehydes and ketones, prepared in situ, were easily converted into dibromoalkenes by treatment with...

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Korotchenko VN, Shastin AV, Nenajdenko VG, et al. Novel efficient synthesis of dibromoalkenes. A first example of catalytic olefination of aliphatic carbonyl compounds. Org Biomol Chem. 2003;1(11):1906-8doi: 10.1039/b303221c.
Korotchenko, V. N., Shastin, A. V., Nenajdenko, V. G., & Balenkova, E. S. (2003). Novel efficient synthesis of dibromoalkenes. A first example of catalytic olefination of aliphatic carbonyl compounds. Organic & biomolecular chemistry, 1(11), 1906-8. https://doi.org/10.1039/b303221c
Korotchenko, Vasily N, et al. "Novel efficient synthesis of dibromoalkenes. A first example of catalytic olefination of aliphatic carbonyl compounds." Organic & biomolecular chemistry vol. 1,11 (2003): 1906-8. doi: https://doi.org/10.1039/b303221c
Korotchenko VN, Shastin AV, Nenajdenko VG, Balenkova ES. Novel efficient synthesis of dibromoalkenes. A first example of catalytic olefination of aliphatic carbonyl compounds. Org Biomol Chem. 2003 Jun 07;1(11):1906-8. doi: 10.1039/b303221c. PMID: 12945772.
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A postgraduate qualification in general practice.

The New Zealand medical journal

VALENTINE J.
PMID: 13924342
N Z Med J. 1961 Sep;60:412-3.

No abstract available.

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VALENTINE J. A postgraduate qualification in general practice. N Z Med J. 1961;60:412-3
VALENTINE, J. (1961). A postgraduate qualification in general practice. The New Zealand medical journal, 60412-3.
VALENTINE, J. "A postgraduate qualification in general practice." The New Zealand medical journal vol. 60 (1961): 412-3.
VALENTINE J. A postgraduate qualification in general practice. N Z Med J. 1961 Sep;60:412-3. PMID: 13924342.
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[Experimental study on the effects of nephro-decapsulation. Determination of the 02 quotient].

Minerva urologica

VALENTINO A, VENERONI G, SORBOLI G.
PMID: 13995866
Minerva Urol. 1962 May-Jun;14:99-100.

No abstract available.

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VALENTINO A, VENERONI G, SORBOLI G. [Experimental study on the effects of nephro-decapsulation. Determination of the 02 quotient]. Minerva Urol. 1962;14:99-100
VALENTINO, A., VENERONI, G., & SORBOLI, G. (1962). [Experimental study on the effects of nephro-decapsulation. Determination of the 02 quotient]. Minerva urologica, 1499-100.
VALENTINO, A, et al. "[Experimental study on the effects of nephro-decapsulation. Determination of the 02 quotient]." Minerva urologica vol. 14 (1962): 99-100.
VALENTINO A, VENERONI G, SORBOLI G. [Experimental study on the effects of nephro-decapsulation. Determination of the 02 quotient]. Minerva Urol. 1962 May-Jun;14:99-100. Italian. PMID: 13995866.
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Teaching aids in clinical psychiatry.

The Journal of mental science

MILLAR WM, VALENTINE M.
PMID: 14938895
J Ment Sci. 1952 Jul;98(412):477-82. doi: 10.1192/bjp.98.412.477.

No abstract available.

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MILLAR WM, VALENTINE M. Teaching aids in clinical psychiatry. J Ment Sci. 1952;98(412):477-82doi: 10.1192/bjp.98.412.477.
MILLAR, W. M., & VALENTINE, M. (1952). Teaching aids in clinical psychiatry. The Journal of mental science, 98(412), 477-82. https://doi.org/10.1192/bjp.98.412.477
MILLAR, W M, and VALENTINE, M. "Teaching aids in clinical psychiatry." The Journal of mental science vol. 98,412 (1952): 477-82. doi: https://doi.org/10.1192/bjp.98.412.477
MILLAR WM, VALENTINE M. Teaching aids in clinical psychiatry. J Ment Sci. 1952 Jul;98(412):477-82. doi: 10.1192/bjp.98.412.477. PMID: 14938895.
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Retraction of an interpretation.

Lancet (London, England)

Murch SH, Anthony A, Casson DH, Malik M, Berelowitz M, Dhillon AP, Thomson MA, Valentine A, Davies SE, Walker-Smith JA.
PMID: 15016483
Lancet. 2004 Mar 06;363(9411):750. doi: 10.1016/S0140-6736(04)15715-2.

No abstract available.

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Murch SH, Anthony A, Casson DH, et al. Retraction of an interpretation. Lancet. 2004;363(9411):750doi: 10.1016/S0140-6736(04)15715-2.
Murch, S. H., Anthony, A., Casson, D. H., Malik, M., Berelowitz, M., Dhillon, A. P., Thomson, M. A., Valentine, A., Davies, S. E., & Walker-Smith, J. A. (2004). Retraction of an interpretation. Lancet (London, England), 363(9411), 750. https://doi.org/10.1016/S0140-6736(04)15715-2
Murch, Simon H, et al. "Retraction of an interpretation." Lancet (London, England) vol. 363,9411 (2004): 750. doi: https://doi.org/10.1016/S0140-6736(04)15715-2
Murch SH, Anthony A, Casson DH, Malik M, Berelowitz M, Dhillon AP, Thomson MA, Valentine A, Davies SE, Walker-Smith JA. Retraction of an interpretation. Lancet. 2004 Mar 06;363(9411):750. doi: 10.1016/S0140-6736(04)15715-2. PMID: 15016483.
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Chiral phosphites derived from carboranes: electronic effect in catalytic asymmetric hydrogenation.

Chirality

Lyubimov SE, Kalinin VN, Tyutyunov AA, Olshevskaya VA, Dutikova YV, Cheong CS, Petrovskii PV, Safronov AS, Davankov VA.
PMID: 18506834
Chirality. 2009 Jan;21(1):2-5. doi: 10.1002/chir.20565.

A series of new fine-tunable monodentate phosphite and phosphoramidite ligands based on carboranes have been synthesized and used for asymmetric Rh-catalyzed hydrogenation of prochiral olefins with the result of up to 99.8% ee. Dependence of the enantioselectivity on the...

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Lyubimov SE, Kalinin VN, Tyutyunov AA, et al. Chiral phosphites derived from carboranes: electronic effect in catalytic asymmetric hydrogenation. Chirality. 2009;21(1):2-5doi: 10.1002/chir.20565.
Lyubimov, S. E., Kalinin, V. N., Tyutyunov, A. A., Olshevskaya, V. A., Dutikova, Y. V., Cheong, C. S., Petrovskii, P. V., Safronov, A. S., & Davankov, V. A. (2009). Chiral phosphites derived from carboranes: electronic effect in catalytic asymmetric hydrogenation. Chirality, 21(1), 2-5. https://doi.org/10.1002/chir.20565
Lyubimov, Sergey E, et al. "Chiral phosphites derived from carboranes: electronic effect in catalytic asymmetric hydrogenation." Chirality vol. 21,1 (2009): 2-5. doi: https://doi.org/10.1002/chir.20565
Lyubimov SE, Kalinin VN, Tyutyunov AA, Olshevskaya VA, Dutikova YV, Cheong CS, Petrovskii PV, Safronov AS, Davankov VA. Chiral phosphites derived from carboranes: electronic effect in catalytic asymmetric hydrogenation. Chirality. 2009 Jan;21(1):2-5. doi: 10.1002/chir.20565. PMID: 18506834.
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Showing 25 to 36 of 837 entries