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Showing 1 to 12 of 190 entries
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The Hairpin Furans: Easily Prepared Hybrids of Helicenes and Twisted Acenes.

Angewandte Chemie (International ed. in English)

Geng X, Donahue JP, Mague JT, Pascal RA.
PMID: 26403622
Angew Chem Int Ed Engl. 2015 Nov 16;54(47):13957-60. doi: 10.1002/anie.201506792. Epub 2015 Sep 25.

The thermal reaction of a cyclopentadienone with 6,6'-dimethoxy-5,5'-binaphthoquinone gives, in a single step, a molecular ribbon consisting of two twisted aromatic systems fused to a heteropentahelicene. Such molecules constitute a new class of chiral polycyclic aromatic compounds, the "hairpin...

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Geng X, Donahue JP, Mague JT, et al. The Hairpin Furans: Easily Prepared Hybrids of Helicenes and Twisted Acenes. Angew Chem Int Ed Engl. 2015;54(47):13957-60doi: 10.1002/anie.201506792.
Geng, X., Donahue, J. P., Mague, J. T., & Pascal, R. A. (2015). The Hairpin Furans: Easily Prepared Hybrids of Helicenes and Twisted Acenes. Angewandte Chemie (International ed. in English), 54(47), 13957-60. https://doi.org/10.1002/anie.201506792
Geng, Xin, et al. "The Hairpin Furans: Easily Prepared Hybrids of Helicenes and Twisted Acenes." Angewandte Chemie (International ed. in English) vol. 54,47 (2015): 13957-60. doi: https://doi.org/10.1002/anie.201506792
Geng X, Donahue JP, Mague JT, Pascal RA. The Hairpin Furans: Easily Prepared Hybrids of Helicenes and Twisted Acenes. Angew Chem Int Ed Engl. 2015 Nov 16;54(47):13957-60. doi: 10.1002/anie.201506792. Epub 2015 Sep 25. PMID: 26403622.
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Response.

Radiology

Radbruch A, Weberling LD, Kieslich PJ, Eidel O, Burth S, Kickingereder P, Wick W, Schlemmer HP, Bendszus M.
PMID: 27437553
Radiology. 2016 Apr;279(1):324-5.

No abstract available.

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Radbruch A, Weberling LD, Kieslich PJ, et al. Response. Radiology. 2016;279(1):324-5
Radbruch, A., Weberling, L. D., Kieslich, P. J., Eidel, O., Burth, S., Kickingereder, P., Wick, W., Schlemmer, H. P., & Bendszus, M. (2016). Response. Radiology, 279(1), 324-5.
Radbruch, Alexander, et al. "Response." Radiology vol. 279,1 (2016): 324-5.
Radbruch A, Weberling LD, Kieslich PJ, Eidel O, Burth S, Kickingereder P, Wick W, Schlemmer HP, Bendszus M. Response. Radiology. 2016 Apr;279(1):324-5. PMID: 27437553.
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A study on the optics of copper indium gallium (di)selenide (CIGS) solar cells with ultra-thin absorber layers.

Optics express

Xu M, Wachters AJ, van Deelen J, Mourad MC, Buskens PJ.
PMID: 24922252
Opt Express. 2014 Mar 10;22:A425-37. doi: 10.1364/OE.22.00A425.

We present a systematic study of the effect of variation of the zinc oxide (ZnO) and copper indium gallium (di)selenide (CIGS) layer thickness on the absorption characteristics of CIGS solar cells using a simulation program based on finite element...

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Xu M, Wachters AJ, van Deelen J, et al. A study on the optics of copper indium gallium (di)selenide (CIGS) solar cells with ultra-thin absorber layers. Opt Express. 2014;22:A425-37doi: 10.1364/OE.22.00A425.
Xu, M., Wachters, A. J., van Deelen, J., Mourad, M. C., & Buskens, P. J. (2014). A study on the optics of copper indium gallium (di)selenide (CIGS) solar cells with ultra-thin absorber layers. Optics express, 22A425-37. https://doi.org/10.1364/OE.22.00A425
Xu, Man, et al. "A study on the optics of copper indium gallium (di)selenide (CIGS) solar cells with ultra-thin absorber layers." Optics express vol. 22 (2014): A425-37. doi: https://doi.org/10.1364/OE.22.00A425
Xu M, Wachters AJ, van Deelen J, Mourad MC, Buskens PJ. A study on the optics of copper indium gallium (di)selenide (CIGS) solar cells with ultra-thin absorber layers. Opt Express. 2014 Mar 10;22:A425-37. doi: 10.1364/OE.22.00A425. PMID: 24922252.
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Syntheses, Crystal Structures, and NLO Properties of New Chiral Inorganic Chromophores for Second-Harmonic Generation.

Inorganic chemistry

Lenoble G, Lacroix PG, Daran JC, Di Bella S, Nakatani K.
PMID: 11670370
Inorg Chem. 1998 May 04;37(9):2158-2165. doi: 10.1021/ic970481w.

A new chiral ligand (H(2)L) based on the condensation of diaminocyclohexane and 4-(diethylamino)salicylaldehyde is reported along with its nickel(II) and manganese(III) complexes. These compounds all crystallize in noncentrosymmetric space groups. Crystal data are as follows. For the ligand (C(28)H(40)N(4)O(2)):...

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Lenoble G, Lacroix PG, Daran JC, et al. Syntheses, Crystal Structures, and NLO Properties of New Chiral Inorganic Chromophores for Second-Harmonic Generation. Inorg Chem. 1998;37(9):2158-2165doi: 10.1021/ic970481w.
Lenoble, G., Lacroix, P. G., Daran, J. C., Di Bella, S., & Nakatani, K. (1998). Syntheses, Crystal Structures, and NLO Properties of New Chiral Inorganic Chromophores for Second-Harmonic Generation. Inorganic chemistry, 37(9), 2158-2165. https://doi.org/10.1021/ic970481w
Lenoble, Géraldine, et al. "Syntheses, Crystal Structures, and NLO Properties of New Chiral Inorganic Chromophores for Second-Harmonic Generation." Inorganic chemistry vol. 37,9 (1998): 2158-2165. doi: https://doi.org/10.1021/ic970481w
Lenoble G, Lacroix PG, Daran JC, Di Bella S, Nakatani K. Syntheses, Crystal Structures, and NLO Properties of New Chiral Inorganic Chromophores for Second-Harmonic Generation. Inorg Chem. 1998 May 04;37(9):2158-2165. doi: 10.1021/ic970481w. PMID: 11670370.
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Directed Evolution and Biocatalysis.

Angewandte Chemie (International ed. in English)

Powell KA, Ramer SW, Del Cardayré SB, Stemmer WP, Tobin MB, Longchamp PF, Huisman GW.
PMID: 12404465
Angew Chem Int Ed Engl. 2001 Nov 05;40(21):3948-3959. doi: 10.1002/1521-3773(20011105)40:21<3948::aid-anie3948>3.0.co;2-n.

This review describes the current state of biocatalysis in the chemical industry. Although we recognize the advantages of chemical approaches, we suggest that the use of biological catalysis is about to expand dramatically because of the recent developments in...

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Powell KA, Ramer SW, Del Cardayré SB, et al. Directed Evolution and Biocatalysis. Angew Chem Int Ed Engl. 2001;40(21):3948-3959doi: 10.1002/1521-3773(20011105)40:21<3948::aid-anie3948>3.0.co;2-n.
Powell, K. A., Ramer, S. W., Del Cardayré, S. B., Stemmer, W. P., Tobin, M. B., Longchamp, P. F., & Huisman, G. W. (2001). Directed Evolution and Biocatalysis. Angewandte Chemie (International ed. in English), 40(21), 3948-3959. https://doi.org/10.1002/1521-3773(20011105)40:21<3948::aid-anie3948>3.0.co;2-n
Powell, Keith A., et al. "Directed Evolution and Biocatalysis." Angewandte Chemie (International ed. in English) vol. 40,21 (2001): 3948-3959. doi: https://doi.org/10.1002/1521-3773(20011105)40:21<3948::aid-anie3948>3.0.co;2-n
Powell KA, Ramer SW, Del Cardayré SB, Stemmer WP, Tobin MB, Longchamp PF, Huisman GW. Directed Evolution and Biocatalysis. Angew Chem Int Ed Engl. 2001 Nov 05;40(21):3948-3959. doi: 10.1002/1521-3773(20011105)40:21<3948::aid-anie3948>3.0.co;2-n. PMID: 12404465.
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A Nearly Linear Single Hydroxo Bridge. Synthesis, Structure, and Magnetic Susceptibility of (&mgr;-Hydroxo)bis((tetraphenylporphinato)manganese(III)) Perchlorate.

Inorganic chemistry

Cheng B, Fries PH, Marchon JC, Scheidt WR.
PMID: 11666280
Inorg Chem. 1996 Feb 14;35(4):1024-1032. doi: 10.1021/ic951041c.

The synthesis, X-ray structure, and magnetic susceptibility characterization of a hydroxo-bridged complex, (&mgr;-hydroxo)bis((tetraphenylporphinato)manganese(III)) perchlorate, {[Mn-(TPP)](2)(OH)}ClO(4), are described. The complex is readily prepared by a controlled hydrolysis of monomeric diaquo(tetraphenylporphinato)manganese(III) perchlorate. Interestingly, the bridging hydroxo complex appears to be more...

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Cheng B, Fries PH, Marchon JC, et al. A Nearly Linear Single Hydroxo Bridge. Synthesis, Structure, and Magnetic Susceptibility of (&mgr;-Hydroxo)bis((tetraphenylporphinato)manganese(III)) Perchlorate. Inorg Chem. 1996;35(4):1024-1032doi: 10.1021/ic951041c.
Cheng, B., Fries, P. H., Marchon, J. C., & Scheidt, W. R. (1996). A Nearly Linear Single Hydroxo Bridge. Synthesis, Structure, and Magnetic Susceptibility of (&mgr;-Hydroxo)bis((tetraphenylporphinato)manganese(III)) Perchlorate. Inorganic chemistry, 35(4), 1024-1032. https://doi.org/10.1021/ic951041c
Cheng, Beisong, et al. "A Nearly Linear Single Hydroxo Bridge. Synthesis, Structure, and Magnetic Susceptibility of (&mgr;-Hydroxo)bis((tetraphenylporphinato)manganese(III)) Perchlorate." Inorganic chemistry vol. 35,4 (1996): 1024-1032. doi: https://doi.org/10.1021/ic951041c
Cheng B, Fries PH, Marchon JC, Scheidt WR. A Nearly Linear Single Hydroxo Bridge. Synthesis, Structure, and Magnetic Susceptibility of (&mgr;-Hydroxo)bis((tetraphenylporphinato)manganese(III)) Perchlorate. Inorg Chem. 1996 Feb 14;35(4):1024-1032. doi: 10.1021/ic951041c. PMID: 11666280.
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Highly efficient P-N nickel(II) complexes for the dimerisation of ethylene.

Chemical communications (Cambridge, England)

Buchard A, Auffrant A, Klemps C, Vu-Do L, Boubekeur L, Goff XF, Floch PL.
PMID: 17406687
Chem Commun (Camb). 2007 Apr 21;(15):1502-4. doi: 10.1039/b618401d. Epub 2007 Feb 05.

New P-N ligands featuring a phosphino group and an iminophosphorane moiety were successfully employed in the nickel-catalysed dimerisation of ethylene.

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Buchard A, Auffrant A, Klemps C, et al. Highly efficient P-N nickel(II) complexes for the dimerisation of ethylene. Chem Commun (Camb). 2007;(15):1502-4doi: 10.1039/b618401d.
Buchard, A., Auffrant, A., Klemps, C., Vu-Do, L., Boubekeur, L., Goff, X. F., & Floch, P. L. (2007). Highly efficient P-N nickel(II) complexes for the dimerisation of ethylene. Chemical communications (Cambridge, England), (15), 1502-4. https://doi.org/10.1039/b618401d
Buchard, Antoine, et al. "Highly efficient P-N nickel(II) complexes for the dimerisation of ethylene." Chemical communications (Cambridge, England) vol. ,15 (2007): 1502-4. doi: https://doi.org/10.1039/b618401d
Buchard A, Auffrant A, Klemps C, Vu-Do L, Boubekeur L, Goff XF, Floch PL. Highly efficient P-N nickel(II) complexes for the dimerisation of ethylene. Chem Commun (Camb). 2007 Apr 21;(15):1502-4. doi: 10.1039/b618401d. Epub 2007 Feb 05. PMID: 17406687.
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Configurationally stable longitudinally twisted polycyclic aromatic compounds.

Journal of the American Chemical Society

Walters RS, Kraml CM, Byrne N, Ho DM, Qin Q, Coughlin FJ, Bernhard S, Pascal RA.
PMID: 18998648
J Am Chem Soc. 2008 Dec 03;130(48):16435-41. doi: 10.1021/ja806958x.

Two strategies for the synthesis of configurationally stable twisted polycyclic aromatic compounds (PACs) were pursued. The first approach employed dissymmetrically positioned 1-naphthyl substituents to bias the direction of twist in highly substituted PACs. 2,3-Bis(1-naphthyl)-1,4-diphenyltriphenylene (7) was prepared, and its...

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Walters RS, Kraml CM, Byrne N, et al. Configurationally stable longitudinally twisted polycyclic aromatic compounds. J Am Chem Soc. 2008;130(48):16435-41doi: 10.1021/ja806958x.
Walters, R. S., Kraml, C. M., Byrne, N., Ho, D. M., Qin, Q., Coughlin, F. J., Bernhard, S., & Pascal, R. A. (2008). Configurationally stable longitudinally twisted polycyclic aromatic compounds. Journal of the American Chemical Society, 130(48), 16435-41. https://doi.org/10.1021/ja806958x
Walters, Robert S, et al. "Configurationally stable longitudinally twisted polycyclic aromatic compounds." Journal of the American Chemical Society vol. 130,48 (2008): 16435-41. doi: https://doi.org/10.1021/ja806958x
Walters RS, Kraml CM, Byrne N, Ho DM, Qin Q, Coughlin FJ, Bernhard S, Pascal RA. Configurationally stable longitudinally twisted polycyclic aromatic compounds. J Am Chem Soc. 2008 Dec 03;130(48):16435-41. doi: 10.1021/ja806958x. PMID: 18998648.
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A study of competitive behavior in mental defectives.

American journal of mental deficiency

ALBEE GW, PASCAL GR.
PMID: 14819090
Am J Ment Defic. 1951 Apr;55(4):576-81.

No abstract available.

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ALBEE GW, PASCAL GR. A study of competitive behavior in mental defectives. Am J Ment Defic. 1951;55(4):576-81
ALBEE, G. W., & PASCAL, G. R. (1951). A study of competitive behavior in mental defectives. American journal of mental deficiency, 55(4), 576-81.
ALBEE, G W, and PASCAL, G R. "A study of competitive behavior in mental defectives." American journal of mental deficiency vol. 55,4 (1951): 576-81.
ALBEE GW, PASCAL GR. A study of competitive behavior in mental defectives. Am J Ment Defic. 1951 Apr;55(4):576-81. PMID: 14819090.
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Sparse canonical methods for biological data integration: application to a cross-platform study.

BMC bioinformatics

Lê Cao KA, Martin PG, Robert-Granié C, Besse P.
PMID: 19171069
BMC Bioinformatics. 2009 Jan 26;10:34. doi: 10.1186/1471-2105-10-34.

BACKGROUND: In the context of systems biology, few sparse approaches have been proposed so far to integrate several data sets. It is however an important and fundamental issue that will be widely encountered in post genomic studies, when simultaneously...

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Lê Cao KA, Martin PG, Robert-Granié C, et al. Sparse canonical methods for biological data integration: application to a cross-platform study. BMC Bioinformatics. 2009;10:34doi: 10.1186/1471-2105-10-34.
Lê Cao, K. A., Martin, P. G., Robert-Granié, C., & Besse, P. (2009). Sparse canonical methods for biological data integration: application to a cross-platform study. BMC bioinformatics, 1034. https://doi.org/10.1186/1471-2105-10-34
Lê Cao, Kim-Anh, et al. "Sparse canonical methods for biological data integration: application to a cross-platform study." BMC bioinformatics vol. 10 (2009): 34. doi: https://doi.org/10.1186/1471-2105-10-34
Lê Cao KA, Martin PG, Robert-Granié C, Besse P. Sparse canonical methods for biological data integration: application to a cross-platform study. BMC Bioinformatics. 2009 Jan 26;10:34. doi: 10.1186/1471-2105-10-34. PMID: 19171069; PMCID: PMC2640358.
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OPHTHALMIC CALCULATIONS BY THE "DAM" METHOD.

The British journal of ophthalmology

Pascal JI.
PMID: 18170364
Br J Ophthalmol. 1947 Jul;31(7):424-6. doi: 10.1136/bjo.31.7.424.

No abstract available.

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Pascal JI. OPHTHALMIC CALCULATIONS BY THE "DAM" METHOD. Br J Ophthalmol. 1947;31(7):424-6doi: 10.1136/bjo.31.7.424.
Pascal, J. I. (1947). OPHTHALMIC CALCULATIONS BY THE "DAM" METHOD. The British journal of ophthalmology, 31(7), 424-6. https://doi.org/10.1136/bjo.31.7.424
Pascal, J I. "OPHTHALMIC CALCULATIONS BY THE "DAM" METHOD." The British journal of ophthalmology vol. 31,7 (1947): 424-6. doi: https://doi.org/10.1136/bjo.31.7.424
Pascal JI. OPHTHALMIC CALCULATIONS BY THE "DAM" METHOD. Br J Ophthalmol. 1947 Jul;31(7):424-6. doi: 10.1136/bjo.31.7.424. PMID: 18170364; PMCID: PMC513863.
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Accelerated luminophore discovery through combinatorial synthesis.

Journal of the American Chemical Society

Lowry MS, Hudson WR, Pascal RA, Bernhard S.
PMID: 15506778
J Am Chem Soc. 2004 Nov 03;126(43):14129-35. doi: 10.1021/ja047156+.

A method for accelerating the discovery of ionic luminophores using combinatorial techniques is reported. The photophysical properties of the resulting transition-metal-based chromophores were compared against a series of analogous, traditionally prepared species. The strong overlap between these two sets...

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Lowry MS, Hudson WR, Pascal RA, et al. Accelerated luminophore discovery through combinatorial synthesis. J Am Chem Soc. 2004;126(43):14129-35doi: 10.1021/ja047156+.
Lowry, M. S., Hudson, W. R., Pascal, R. A., & Bernhard, S. (2004). Accelerated luminophore discovery through combinatorial synthesis. Journal of the American Chemical Society, 126(43), 14129-35. https://doi.org/10.1021/ja047156+
Lowry, Michael S, et al. "Accelerated luminophore discovery through combinatorial synthesis." Journal of the American Chemical Society vol. 126,43 (2004): 14129-35. doi: https://doi.org/10.1021/ja047156+
Lowry MS, Hudson WR, Pascal RA, Bernhard S. Accelerated luminophore discovery through combinatorial synthesis. J Am Chem Soc. 2004 Nov 03;126(43):14129-35. doi: 10.1021/ja047156+. PMID: 15506778.
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Showing 1 to 12 of 190 entries