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Showing 1 to 12 of 16 entries
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Ultralow-loss 3-dB photonic crystal waveguide splitter.

Optics letters

Frandsen LH, Borel PI, Zhuang YX, Harpøth A, Thorhauge M, Kristensen M, Bogaerts W, Dumon P, Baets R, Wiaux V, Wouters J, Beckx S.
PMID: 15309839
Opt Lett. 2004 Jul 15;29(14):1623-5. doi: 10.1364/ol.29.001623.

A photonic crystal waveguide splitter that exhibits ultralow-loss 3-dB splitting for TE-polarized light is fabricated in silicon-on-insulator material by use of deep UV lithography. The high performance is achieved by use of a Y junction, which is designed to...

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Frandsen LH, Borel PI, Zhuang YX, et al. Ultralow-loss 3-dB photonic crystal waveguide splitter. Opt Lett. 2004;29(14):1623-5doi: 10.1364/ol.29.001623.
Frandsen, L. H., Borel, P. I., Zhuang, Y. X., Harpøth, A., Thorhauge, M., Kristensen, M., Bogaerts, W., Dumon, P., Baets, R., Wiaux, V., Wouters, J., & Beckx, S. (2004). Ultralow-loss 3-dB photonic crystal waveguide splitter. Optics letters, 29(14), 1623-5. https://doi.org/10.1364/ol.29.001623
Frandsen, L H, et al. "Ultralow-loss 3-dB photonic crystal waveguide splitter." Optics letters vol. 29,14 (2004): 1623-5. doi: https://doi.org/10.1364/ol.29.001623
Frandsen LH, Borel PI, Zhuang YX, Harpøth A, Thorhauge M, Kristensen M, Bogaerts W, Dumon P, Baets R, Wiaux V, Wouters J, Beckx S. Ultralow-loss 3-dB photonic crystal waveguide splitter. Opt Lett. 2004 Jul 15;29(14):1623-5. doi: 10.1364/ol.29.001623. PMID: 15309839.
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Efficient propagation of TM polarized light in photonic crystal components exhibiting band gaps for TE polarized light.

Optics express

Borel P, Frandsen L, Thorhauge M, Harpøth A, Zhuang Y, Kristensen M, Chong H.
PMID: 19466056
Opt Express. 2003 Jul 28;11(15):1757-62. doi: 10.1364/oe.11.001757.

We have investigated the properties of TM polarized light in planar photonic crystal waveguide structures, which exhibit photonic band gaps for TE polarized light. Straight and bent photonic crystal waveguides and couplers have been fabricated in silicon-on-insulator material and...

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Borel P, Frandsen L, Thorhauge M, et al. Efficient propagation of TM polarized light in photonic crystal components exhibiting band gaps for TE polarized light. Opt Express. 2003;11(15):1757-62doi: 10.1364/oe.11.001757.
Borel, P., Frandsen, L., Thorhauge, M., Harpøth, A., Zhuang, Y., Kristensen, M., & Chong, H. (2003). Efficient propagation of TM polarized light in photonic crystal components exhibiting band gaps for TE polarized light. Optics express, 11(15), 1757-62. https://doi.org/10.1364/oe.11.001757
Borel, P, et al. "Efficient propagation of TM polarized light in photonic crystal components exhibiting band gaps for TE polarized light." Optics express vol. 11,15 (2003): 1757-62. doi: https://doi.org/10.1364/oe.11.001757
Borel P, Frandsen L, Thorhauge M, Harpøth A, Zhuang Y, Kristensen M, Chong H. Efficient propagation of TM polarized light in photonic crystal components exhibiting band gaps for TE polarized light. Opt Express. 2003 Jul 28;11(15):1757-62. doi: 10.1364/oe.11.001757. PMID: 19466056.
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Highly Enantioselective Catalytic Hetero-Diels-Alder Reaction with Inverse Electron Demand.

Angewandte Chemie (International ed. in English)

Thorhauge J, Johannsen M, Jørgensen KA.
PMID: 29710966
Angew Chem Int Ed Engl. 1998 Sep 18;37(17):2404-2406. doi: 10.1002/(SICI)1521-3773(19980918)37:17<2404::AID-ANIE2404>3.0.CO;2-D.

Valuable substrates for the synthesis of natural products, compounds 3 (R

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Thorhauge J, Johannsen M, Jørgensen KA. Highly Enantioselective Catalytic Hetero-Diels-Alder Reaction with Inverse Electron Demand. Angew Chem Int Ed Engl. 1998;37(17):2404-2406doi: 10.1002/(SICI)1521-3773(19980918)37:17<2404::AID-ANIE2404>3.0.CO;2-D.
Thorhauge, J., Johannsen, M., & Jørgensen, K. A. (1998). Highly Enantioselective Catalytic Hetero-Diels-Alder Reaction with Inverse Electron Demand. Angewandte Chemie (International ed. in English), 37(17), 2404-2406. https://doi.org/10.1002/(SICI)1521-3773(19980918)37:17<2404::AID-ANIE2404>3.0.CO;2-D
Thorhauge, Jacob, et al. "Highly Enantioselective Catalytic Hetero-Diels-Alder Reaction with Inverse Electron Demand." Angewandte Chemie (International ed. in English) vol. 37,17 (1998): 2404-2406. doi: https://doi.org/10.1002/(SICI)1521-3773(19980918)37:17<2404::AID-ANIE2404>3.0.CO;2-D
Thorhauge J, Johannsen M, Jørgensen KA. Highly Enantioselective Catalytic Hetero-Diels-Alder Reaction with Inverse Electron Demand. Angew Chem Int Ed Engl. 1998 Sep 18;37(17):2404-2406. doi: 10.1002/(SICI)1521-3773(19980918)37:17<2404::AID-ANIE2404>3.0.CO;2-D. PMID: 29710966.
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The influence of acceptor and donor doping on the protonic surface conduction of TiO.

Physical chemistry chemical physics : PCCP

Stub SØ, Thorshaug K, Rørvik PM, Norby T, Vøllestad E.
PMID: 29845151
Phys Chem Chem Phys. 2018 Jun 13;20(23):15653-15660. doi: 10.1039/c8cp00571k.

The transport of protonic charge carriers along and within the pore surfaces of porous oxide matrices is of significant importance for many catalytic and electrochemical applications, with porous TiO2 being a candidate material both for photocatalytic applications and as...

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Stub SØ, Thorshaug K, Rørvik PM, et al. The influence of acceptor and donor doping on the protonic surface conduction of TiO. Phys Chem Chem Phys. 2018;20(23):15653-15660doi: 10.1039/c8cp00571k.
Stub, S. �. �., Thorshaug, K., Rørvik, P. M., Norby, T., & Vøllestad, E. (2018). The influence of acceptor and donor doping on the protonic surface conduction of TiO. Physical chemistry chemical physics : PCCP, 20(23), 15653-15660. https://doi.org/10.1039/c8cp00571k
Stub, Sindre Østby, et al. "The influence of acceptor and donor doping on the protonic surface conduction of TiO." Physical chemistry chemical physics : PCCP vol. 20,23 (2018): 15653-15660. doi: https://doi.org/10.1039/c8cp00571k
Stub SØ, Thorshaug K, Rørvik PM, Norby T, Vøllestad E. The influence of acceptor and donor doping on the protonic surface conduction of TiO. Phys Chem Chem Phys. 2018 Jun 13;20(23):15653-15660. doi: 10.1039/c8cp00571k. PMID: 29845151.
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On the intermediates in chiral bis(oxazoline)copper(II)-catalyzed enantioselective reactions--experimental and theoretical investigations.

Chemistry (Weinheim an der Bergstrasse, Germany)

Thorhauge J, Roberson M, Hazell RG, Jørgensen KA.
PMID: 12007099
Chemistry. 2002 Apr 15;8(8):1888-98. doi: 10.1002/1521-3765(20020415)8:8<1888::AID-CHEM1888>3.0.CO;2-9.

The intermediates in the chiral bis(oxazoline)copper(II)-catalyzed reactions have been investigated by means of experimental and theoretical investigations. It is shown that the absolute configuration of the hetero-Diels-Alder adduct obtained from the reaction of ethyl glyoxylate with 1,3-cyclohexadiene in the...

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Thorhauge J, Roberson M, Hazell RG, et al. On the intermediates in chiral bis(oxazoline)copper(II)-catalyzed enantioselective reactions--experimental and theoretical investigations. Chemistry. 2002;8(8):1888-98doi: 10.1002/1521-3765(20020415)8:8<1888::AID-CHEM1888>3.0.CO;2-9.
Thorhauge, J., Roberson, M., Hazell, R. G., & Jørgensen, K. A. (2002). On the intermediates in chiral bis(oxazoline)copper(II)-catalyzed enantioselective reactions--experimental and theoretical investigations. Chemistry (Weinheim an der Bergstrasse, Germany), 8(8), 1888-98. https://doi.org/10.1002/1521-3765(20020415)8:8<1888::AID-CHEM1888>3.0.CO;2-9
Thorhauge, Jacob, et al. "On the intermediates in chiral bis(oxazoline)copper(II)-catalyzed enantioselective reactions--experimental and theoretical investigations." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 8,8 (2002): 1888-98. doi: https://doi.org/10.1002/1521-3765(20020415)8:8<1888::AID-CHEM1888>3.0.CO;2-9
Thorhauge J, Roberson M, Hazell RG, Jørgensen KA. On the intermediates in chiral bis(oxazoline)copper(II)-catalyzed enantioselective reactions--experimental and theoretical investigations. Chemistry. 2002 Apr 15;8(8):1888-98. doi: 10.1002/1521-3765(20020415)8:8<1888::AID-CHEM1888>3.0.CO;2-9. PMID: 12007099.
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Quantifying the promotion of Cu catalysts by ZnO for methanol synthesis.

Science (New York, N.Y.)

Kuld S, Thorhauge M, Falsig H, Elkjær CF, Helveg S, Chorkendorff I, Sehested J.
PMID: 27199425
Science. 2016 May 20;352(6288):969-74. doi: 10.1126/science.aaf0718.

Promoter elements enhance the activity and selectivity of heterogeneous catalysts. Here, we show how methanol synthesis from synthesis gas over copper (Cu) nanoparticles is boosted by zinc oxide (ZnO) nanoparticles. By combining surface area titration, electron microscopy, activity measurement,...

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Kuld S, Thorhauge M, Falsig H, et al. Quantifying the promotion of Cu catalysts by ZnO for methanol synthesis. Science. 2016;352(6288):969-74doi: 10.1126/science.aaf0718.
Kuld, S., Thorhauge, M., Falsig, H., Elkjær, C. F., Helveg, S., Chorkendorff, I., & Sehested, J. (2016). Quantifying the promotion of Cu catalysts by ZnO for methanol synthesis. Science (New York, N.Y.), 352(6288), 969-74. https://doi.org/10.1126/science.aaf0718
Kuld, Sebastian, et al. "Quantifying the promotion of Cu catalysts by ZnO for methanol synthesis." Science (New York, N.Y.) vol. 352,6288 (2016): 969-74. doi: https://doi.org/10.1126/science.aaf0718
Kuld S, Thorhauge M, Falsig H, Elkjær CF, Helveg S, Chorkendorff I, Sehested J. Quantifying the promotion of Cu catalysts by ZnO for methanol synthesis. Science. 2016 May 20;352(6288):969-74. doi: 10.1126/science.aaf0718. PMID: 27199425.
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To drive or not to drive? A study of travel behavior for a recent drinking occasion.

Travel behaviour & society

MacLeod KE, Thorhauge M, Villalobos V, van Meijgaard J, Karriker-Jaffe KJ, Kelley-Baker T, Ragland DR.
PMID: 34703766
Travel Behav Soc. 2020 Jul;20:74-82. doi: 10.1016/j.tbs.2020.02.008. Epub 2020 Mar 05.

Despite decades of education and enforcement campaigns, alcohol-impaired driving persists as a social problem in the U.S. Are there other factors influencing decisions to drive after alcohol consumption that may be amenable to change? We conducted a roadside survey...

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MacLeod KE, Thorhauge M, Villalobos V, et al. To drive or not to drive? A study of travel behavior for a recent drinking occasion. Travel Behav Soc. 2020;20:74-82doi: 10.1016/j.tbs.2020.02.008.
MacLeod, K. E., Thorhauge, M., Villalobos, V., van Meijgaard, J., Karriker-Jaffe, K. J., Kelley-Baker, T., & Ragland, D. R. (2020). To drive or not to drive? A study of travel behavior for a recent drinking occasion. Travel behaviour & society, 2074-82. https://doi.org/10.1016/j.tbs.2020.02.008
MacLeod, Kara E, et al. "To drive or not to drive? A study of travel behavior for a recent drinking occasion." Travel behaviour & society vol. 20 (2020): 74-82. doi: https://doi.org/10.1016/j.tbs.2020.02.008
MacLeod KE, Thorhauge M, Villalobos V, van Meijgaard J, Karriker-Jaffe KJ, Kelley-Baker T, Ragland DR. To drive or not to drive? A study of travel behavior for a recent drinking occasion. Travel Behav Soc. 2020 Jul;20:74-82. doi: 10.1016/j.tbs.2020.02.008. Epub 2020 Mar 05. PMID: 34703766; PMCID: PMC8545274.
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In situ infrared emission spectroscopy for quantitative gas-phase measurement under high temperature reaction conditions: an analytical method for methane by means of an innovative small-volume flowing cell.

Applied spectroscopy

Usseglio S, Thorshaug K, Karlsson A, Dahl IM, Nielsen CJ, Jens KJ, Tangstad E.
PMID: 20149274
Appl Spectrosc. 2010 Feb;64(2):141-8. doi: 10.1366/000370210790619564.

We have used infrared emission spectroscopy (IRES) in order to perform in situ studies under flowing gas-phase conditions. When the small-volume cell developed herein is used, we can (1) observe emission spectra from a hot gas-phase sample having an...

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Usseglio S, Thorshaug K, Karlsson A, et al. In situ infrared emission spectroscopy for quantitative gas-phase measurement under high temperature reaction conditions: an analytical method for methane by means of an innovative small-volume flowing cell. Appl Spectrosc. 2010;64(2):141-8doi: 10.1366/000370210790619564.
Usseglio, S., Thorshaug, K., Karlsson, A., Dahl, I. M., Nielsen, C. J., Jens, K. J., & Tangstad, E. (2010). In situ infrared emission spectroscopy for quantitative gas-phase measurement under high temperature reaction conditions: an analytical method for methane by means of an innovative small-volume flowing cell. Applied spectroscopy, 64(2), 141-8. https://doi.org/10.1366/000370210790619564
Usseglio, Sandro, et al. "In situ infrared emission spectroscopy for quantitative gas-phase measurement under high temperature reaction conditions: an analytical method for methane by means of an innovative small-volume flowing cell." Applied spectroscopy vol. 64,2 (2010): 141-8. doi: https://doi.org/10.1366/000370210790619564
Usseglio S, Thorshaug K, Karlsson A, Dahl IM, Nielsen CJ, Jens KJ, Tangstad E. In situ infrared emission spectroscopy for quantitative gas-phase measurement under high temperature reaction conditions: an analytical method for methane by means of an innovative small-volume flowing cell. Appl Spectrosc. 2010 Feb;64(2):141-8. doi: 10.1366/000370210790619564. PMID: 20149274.
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Efficient photonic crystal directional couplers.

Optics letters

Thorhauge M, Frandsen LH, Borel PI.
PMID: 12956367
Opt Lett. 2003 Sep 01;28(17):1525-7. doi: 10.1364/ol.28.001525.

We demonstrate highly efficient and spectrally flat broadband coupling in photonic crystal directional couplers. The result is obtained by use of a novel design with smaller holes between coparallel photonic crystal waveguides for efficient channel-to-channel coupling. The system studied...

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Thorhauge M, Frandsen LH, Borel PI. Efficient photonic crystal directional couplers. Opt Lett. 2003;28(17):1525-7doi: 10.1364/ol.28.001525.
Thorhauge, M., Frandsen, L. H., & Borel, P. I. (2003). Efficient photonic crystal directional couplers. Optics letters, 28(17), 1525-7. https://doi.org/10.1364/ol.28.001525
Thorhauge, Morten, et al. "Efficient photonic crystal directional couplers." Optics letters vol. 28,17 (2003): 1525-7. doi: https://doi.org/10.1364/ol.28.001525
Thorhauge M, Frandsen LH, Borel PI. Efficient photonic crystal directional couplers. Opt Lett. 2003 Sep 01;28(17):1525-7. doi: 10.1364/ol.28.001525. PMID: 12956367.
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Catalytic Asymmetric Friedel-Crafts Alkylation of β,γ-Unsaturated α-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes.

Angewandte Chemie (International ed. in English)

Jensen KB, Thorhauge J, Hazell RG, Jørgensen KA.
PMID: 29711935
Angew Chem Int Ed Engl. 2001 Jan 05;40(1):160-163. doi: 10.1002/1521-3773(20010105)40:1<160::AID-ANIE160>3.0.CO;2-S.

No abstract available.

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Jensen KB, Thorhauge J, Hazell RG, et al. Catalytic Asymmetric Friedel-Crafts Alkylation of β,γ-Unsaturated α-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes. Angew Chem Int Ed Engl. 2001;40(1):160-163doi: 10.1002/1521-3773(20010105)40:1<160::AID-ANIE160>3.0.CO;2-S.
Jensen, K. B., Thorhauge, J., Hazell, R. G., & Jørgensen, K. A. (2001). Catalytic Asymmetric Friedel-Crafts Alkylation of β,γ-Unsaturated α-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes. Angewandte Chemie (International ed. in English), 40(1), 160-163. https://doi.org/10.1002/1521-3773(20010105)40:1<160::AID-ANIE160>3.0.CO;2-S
Jensen, Kim B, et al. "Catalytic Asymmetric Friedel-Crafts Alkylation of β,γ-Unsaturated α-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes." Angewandte Chemie (International ed. in English) vol. 40,1 (2001): 160-163. doi: https://doi.org/10.1002/1521-3773(20010105)40:1<160::AID-ANIE160>3.0.CO;2-S
Jensen KB, Thorhauge J, Hazell RG, Jørgensen KA. Catalytic Asymmetric Friedel-Crafts Alkylation of β,γ-Unsaturated α-Ketoesters: Enantioselective Addition of Aromatic C-H Bonds to Alkenes. Angew Chem Int Ed Engl. 2001 Jan 05;40(1):160-163. doi: 10.1002/1521-3773(20010105)40:1<160::AID-ANIE160>3.0.CO;2-S. PMID: 29711935.
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An experimental and theoretical study of spin-spin coupling in chlorosilanes.

The journal of physical chemistry. A

Thorshaug K, Swang O, Dahl IM, Olafsen A.
PMID: 16898680
J Phys Chem A. 2006 Aug 17;110(32):9801-4. doi: 10.1021/jp060704g.

An experimental and theoretical study of the absolute value of the one-bond spin-spin coupling constant |(1)J(Si,H)| in SiH(n)Cl(4-n) (n = 0-4) dissolved in THF-d(8) is presented. We found |(1)J(Si,H)| to increase with an increasing number of chlorine substituents, and...

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Thorshaug K, Swang O, Dahl IM, et al. An experimental and theoretical study of spin-spin coupling in chlorosilanes. J Phys Chem A. 2006;110(32):9801-4doi: 10.1021/jp060704g.
Thorshaug, K., Swang, O., Dahl, I. M., & Olafsen, A. (2006). An experimental and theoretical study of spin-spin coupling in chlorosilanes. The journal of physical chemistry. A, 110(32), 9801-4. https://doi.org/10.1021/jp060704g
Thorshaug, Knut, et al. "An experimental and theoretical study of spin-spin coupling in chlorosilanes." The journal of physical chemistry. A vol. 110,32 (2006): 9801-4. doi: https://doi.org/10.1021/jp060704g
Thorshaug K, Swang O, Dahl IM, Olafsen A. An experimental and theoretical study of spin-spin coupling in chlorosilanes. J Phys Chem A. 2006 Aug 17;110(32):9801-4. doi: 10.1021/jp060704g. PMID: 16898680.
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Linker conformation effects on the band gap in metal-organic frameworks.

Inorganic chemistry

Flage-Larsen E, Thorshaug K.
PMID: 24528111
Inorg Chem. 2014 Mar 03;53(5):2569-72. doi: 10.1021/ic4028628. Epub 2014 Feb 14.

In this work, we investigate how torsion in the middle aromatic ring on the terphenyldicarboxylate linker in UiO-68 affects the band gap. Furthermore, we incorporate the effect of monosubstitution on the linker (UiO-68-R; R = H, F, I, NH2,...

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Flage-Larsen E, Thorshaug K. Linker conformation effects on the band gap in metal-organic frameworks. Inorg Chem. 2014;53(5):2569-72doi: 10.1021/ic4028628.
Flage-Larsen, E., & Thorshaug, K. (2014). Linker conformation effects on the band gap in metal-organic frameworks. Inorganic chemistry, 53(5), 2569-72. https://doi.org/10.1021/ic4028628
Flage-Larsen, Espen, and Thorshaug, Knut. "Linker conformation effects on the band gap in metal-organic frameworks." Inorganic chemistry vol. 53,5 (2014): 2569-72. doi: https://doi.org/10.1021/ic4028628
Flage-Larsen E, Thorshaug K. Linker conformation effects on the band gap in metal-organic frameworks. Inorg Chem. 2014 Mar 03;53(5):2569-72. doi: 10.1021/ic4028628. Epub 2014 Feb 14. PMID: 24528111.
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