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Showing 1 to 12 of 112 entries
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Superconductivity in transition metals.

Philosophical transactions. Series A, Mathematical, physical, and engineering sciences

Slocombe DR, Kuznetsov VL, Grochala W, Williams RJ, Edwards PP.
PMID: 25666075
Philos Trans A Math Phys Eng Sci. 2015 Mar 13;373(2037). doi: 10.1098/rsta.2014.0476.

A qualitative account of the occurrence and magnitude of superconductivity in the transition metals is presented, with a primary emphasis on elements of the first row. Correlations of the important parameters of the Bardeen-Cooper-Schrieffer theory of superconductivity are highlighted...

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Slocombe DR, Kuznetsov VL, Grochala W, et al. Superconductivity in transition metals. Philos Trans A Math Phys Eng Sci. 2015;373(2037)doi: 10.1098/rsta.2014.0476.
Slocombe, D. R., Kuznetsov, V. L., Grochala, W., Williams, R. J., & Edwards, P. P. (2015). Superconductivity in transition metals. Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 373(2037), . https://doi.org/10.1098/rsta.2014.0476
Slocombe, Daniel R, et al. "Superconductivity in transition metals." Philosophical transactions. Series A, Mathematical, physical, and engineering sciences vol. 373,2037 (2015). doi: https://doi.org/10.1098/rsta.2014.0476
Slocombe DR, Kuznetsov VL, Grochala W, Williams RJ, Edwards PP. Superconductivity in transition metals. Philos Trans A Math Phys Eng Sci. 2015 Mar 13;373(2037). doi: 10.1098/rsta.2014.0476. PMID: 25666075.
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Bioorthogonal catalysis: Rise of the nanobots.

Nature chemistry

Unciti-Broceta A.
PMID: 26100798
Nat Chem. 2015 Jul;7(7):538-9. doi: 10.1038/nchem.2291.

No abstract available.

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Unciti-Broceta A. Bioorthogonal catalysis: Rise of the nanobots. Nat Chem. 2015;7(7):538-9doi: 10.1038/nchem.2291.
Unciti-Broceta, A. (2015). Bioorthogonal catalysis: Rise of the nanobots. Nature chemistry, 7(7), 538-9. https://doi.org/10.1038/nchem.2291
Unciti-Broceta, Asier. "Bioorthogonal catalysis: Rise of the nanobots." Nature chemistry vol. 7,7 (2015): 538-9. doi: https://doi.org/10.1038/nchem.2291
Unciti-Broceta A. Bioorthogonal catalysis: Rise of the nanobots. Nat Chem. 2015 Jul;7(7):538-9. doi: 10.1038/nchem.2291. PMID: 26100798.
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Highly Polar Metal-Metal Bonds in "Early-Late" Heterodimetallic Complexes.

Angewandte Chemie (International ed. in English)

Gade LH.
PMID: 10934392
Angew Chem Int Ed Engl. 2000 Aug 04;39(15):2658-2678. doi: 10.1002/1521-3773(20000804)39:15<2658::aid-anie2658>3.0.co;2-c.

Metal-metal bond polarity in its extreme form involving transition elements is found in di- or polynuclear complexes in which molecular fragments containing metal atoms from the two ends of the d block in the periodic table are combined. This...

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Gade LH. Highly Polar Metal-Metal Bonds in "Early-Late" Heterodimetallic Complexes. Angew Chem Int Ed Engl. 2000;39(15):2658-2678doi: 10.1002/1521-3773(20000804)39:15<2658::aid-anie2658>3.0.co;2-c.
Gade, L. H. (2000). Highly Polar Metal-Metal Bonds in "Early-Late" Heterodimetallic Complexes. Angewandte Chemie (International ed. in English), 39(15), 2658-2678. https://doi.org/10.1002/1521-3773(20000804)39:15<2658::aid-anie2658>3.0.co;2-c
Gade. "Highly Polar Metal-Metal Bonds in "Early-Late" Heterodimetallic Complexes." Angewandte Chemie (International ed. in English) vol. 39,15 (2000): 2658-2678. doi: https://doi.org/10.1002/1521-3773(20000804)39:15<2658::aid-anie2658>3.0.co;2-c
Gade LH. Highly Polar Metal-Metal Bonds in "Early-Late" Heterodimetallic Complexes. Angew Chem Int Ed Engl. 2000 Aug 04;39(15):2658-2678. doi: 10.1002/1521-3773(20000804)39:15<2658::aid-anie2658>3.0.co;2-c. PMID: 10934392.
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EELS analysis of cation valence states and oxygen vacancies in magnetic oxides.

Micron (Oxford, England : 1993)

Wang ZL, Yin JS, Jiang YD.
PMID: 10831303
Micron. 2000 Oct;31(5):571-80. doi: 10.1016/s0968-4328(99)00139-0.

Transition metal oxides are a class of materials that are vitally important for developing new materials with functionality and smartness. The unique properties of these materials are related to the presence of elements with mixed valences of transition elements....

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Wang ZL, Yin JS, Jiang YD. EELS analysis of cation valence states and oxygen vacancies in magnetic oxides. Micron. 2000;31(5):571-80doi: 10.1016/s0968-4328(99)00139-0.
Wang, Z. L., Yin, J. S., & Jiang, Y. D. (2000). EELS analysis of cation valence states and oxygen vacancies in magnetic oxides. Micron (Oxford, England : 1993), 31(5), 571-80. https://doi.org/10.1016/s0968-4328(99)00139-0
Wang, et al. "EELS analysis of cation valence states and oxygen vacancies in magnetic oxides." Micron (Oxford, England : 1993) vol. 31,5 (2000): 571-80. doi: https://doi.org/10.1016/s0968-4328(99)00139-0
Wang ZL, Yin JS, Jiang YD. EELS analysis of cation valence states and oxygen vacancies in magnetic oxides. Micron. 2000 Oct;31(5):571-80. doi: 10.1016/s0968-4328(99)00139-0. PMID: 10831303.
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On the performance of two-component energy-consistent pseudopotentials in atomic Fock-space coupled cluster calculations.

The Journal of chemical physics

Figgen D, Wedig A, Stoll H, Dolg M, Eliav E, Kaldor U.
PMID: 18205442
J Chem Phys. 2008 Jan 14;128(2):024106. doi: 10.1063/1.2823053.

The four-component atomic intermediate-Hamiltonian Fock-space coupled cluster (IHFSCC) code of Landau et al. [J. Chem. Phys. 115, 6862 (2001)] has been adapted to two-component calculations with relativistic pseudopotentials of the energy-consistent variety. Recently adjusted energy-consistent pseudopotentials for group 11...

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Figgen D, Wedig A, Stoll H, et al. On the performance of two-component energy-consistent pseudopotentials in atomic Fock-space coupled cluster calculations. J Chem Phys. 2008;128(2):024106doi: 10.1063/1.2823053.
Figgen, D., Wedig, A., Stoll, H., Dolg, M., Eliav, E., & Kaldor, U. (2008). On the performance of two-component energy-consistent pseudopotentials in atomic Fock-space coupled cluster calculations. The Journal of chemical physics, 128(2), 024106. https://doi.org/10.1063/1.2823053
Figgen, Detlev, et al. "On the performance of two-component energy-consistent pseudopotentials in atomic Fock-space coupled cluster calculations." The Journal of chemical physics vol. 128,2 (2008): 024106. doi: https://doi.org/10.1063/1.2823053
Figgen D, Wedig A, Stoll H, Dolg M, Eliav E, Kaldor U. On the performance of two-component energy-consistent pseudopotentials in atomic Fock-space coupled cluster calculations. J Chem Phys. 2008 Jan 14;128(2):024106. doi: 10.1063/1.2823053. PMID: 18205442.
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High-temperature molecular magnets based on cyanovanadate building blocks: spontaneous magnetization at 230 k.

Science (New York, N.Y.)

Entley WR, Girolami GS.
PMID: 17746547
Science. 1995 Apr 21;268(5209):397-400. doi: 10.1126/science.268.5209.397.

The molecular-based magnetic materials Cs(2)Mn(||)[V(||)(CN)(6)] (1) and (Et(4)N)(0.5)Mn(l.25)- [V(CN)(5)].2H(2)O (2) (where Et is ethyl) were prepared by the addition of manganese(II) triflate to aqueous solutions of the hexacyanovanadate(II) ion at 0 degrees C. Whereas 1 crystallizes in a face-centered...

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Entley WR, Girolami GS. High-temperature molecular magnets based on cyanovanadate building blocks: spontaneous magnetization at 230 k. Science. 1995;268(5209):397-400doi: 10.1126/science.268.5209.397.
Entley, W. R., & Girolami, G. S. (1995). High-temperature molecular magnets based on cyanovanadate building blocks: spontaneous magnetization at 230 k. Science (New York, N.Y.), 268(5209), 397-400. https://doi.org/10.1126/science.268.5209.397
Entley, W R, and Girolami, G S. "High-temperature molecular magnets based on cyanovanadate building blocks: spontaneous magnetization at 230 k." Science (New York, N.Y.) vol. 268,5209 (1995): 397-400. doi: https://doi.org/10.1126/science.268.5209.397
Entley WR, Girolami GS. High-temperature molecular magnets based on cyanovanadate building blocks: spontaneous magnetization at 230 k. Science. 1995 Apr 21;268(5209):397-400. doi: 10.1126/science.268.5209.397. PMID: 17746547.
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Interaction of the early 3d transition metals Sc, Ti, V, and Cr with N2: an ab initio study.

The Journal of chemical physics

Kardahakis S, Koukounas C, Mavridis A.
PMID: 16542078
J Chem Phys. 2006 Mar 14;124(10):104306. doi: 10.1063/1.2174000.

The interaction of the early 3d transition elements M=Sc, Ti, V, and Cr with N2(X 1Sigmag+) has been studied by coupled-cluster and multiconfigurational techniques in conjunction with quantitative basis sets. We investigated both triatomic (MN2) and tetratomic (M2N2) species...

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Kardahakis S, Koukounas C, Mavridis A. Interaction of the early 3d transition metals Sc, Ti, V, and Cr with N2: an ab initio study. J Chem Phys. 2006;124(10):104306doi: 10.1063/1.2174000.
Kardahakis, S., Koukounas, C., & Mavridis, A. (2006). Interaction of the early 3d transition metals Sc, Ti, V, and Cr with N2: an ab initio study. The Journal of chemical physics, 124(10), 104306. https://doi.org/10.1063/1.2174000
Kardahakis, Stavros, et al. "Interaction of the early 3d transition metals Sc, Ti, V, and Cr with N2: an ab initio study." The Journal of chemical physics vol. 124,10 (2006): 104306. doi: https://doi.org/10.1063/1.2174000
Kardahakis S, Koukounas C, Mavridis A. Interaction of the early 3d transition metals Sc, Ti, V, and Cr with N2: an ab initio study. J Chem Phys. 2006 Mar 14;124(10):104306. doi: 10.1063/1.2174000. PMID: 16542078.
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Adsorption of chloro-complexes of the first row transition elements by Dowex A-1.

Talanta

Birney DG, Blake WE, Meldrum PR, Peach ME.
PMID: 18960332
Talanta. 1968 Jun;15(6):557-9. doi: 10.1016/0039-9140(68)80130-4.

A study has been made of the adsorption of chlorocomplexes of the first row transition metals by the chelating resin Dowex A-1, and possible mechanisms for adsorption have been reviewed. Relative adsorption follows the series Zn(II) > Co(II) =...

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Birney DG, Blake WE, Meldrum PR, et al. Adsorption of chloro-complexes of the first row transition elements by Dowex A-1. Talanta. 1968;15(6):557-9doi: 10.1016/0039-9140(68)80130-4.
Birney, D. G., Blake, W. E., Meldrum, P. R., & Peach, M. E. (1968). Adsorption of chloro-complexes of the first row transition elements by Dowex A-1. Talanta, 15(6), 557-9. https://doi.org/10.1016/0039-9140(68)80130-4
Birney, D G, et al. "Adsorption of chloro-complexes of the first row transition elements by Dowex A-1." Talanta vol. 15,6 (1968): 557-9. doi: https://doi.org/10.1016/0039-9140(68)80130-4
Birney DG, Blake WE, Meldrum PR, Peach ME. Adsorption of chloro-complexes of the first row transition elements by Dowex A-1. Talanta. 1968 Jun;15(6):557-9. doi: 10.1016/0039-9140(68)80130-4. PMID: 18960332.
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Metal oxide chemistry in solution: the early transition metal polyoxoanions.

Science (New York, N.Y.)

Day VW, Klemperer WG.
PMID: 17736064
Science. 1985 May 03;228(4699):533-41. doi: 10.1126/science.228.4699.533.

Many of the early transition elements form large polynuclear metal-oxygen anions containing up to 200 atoms or more. Although these polyoxoanions have been investigated for more than a century, detailed studies of structure and reactivity were not possible until...

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Day VW, Klemperer WG. Metal oxide chemistry in solution: the early transition metal polyoxoanions. Science. 1985;228(4699):533-41doi: 10.1126/science.228.4699.533.
Day, V. W., & Klemperer, W. G. (1985). Metal oxide chemistry in solution: the early transition metal polyoxoanions. Science (New York, N.Y.), 228(4699), 533-41. https://doi.org/10.1126/science.228.4699.533
Day, V W, and Klemperer, W G. "Metal oxide chemistry in solution: the early transition metal polyoxoanions." Science (New York, N.Y.) vol. 228,4699 (1985): 533-41. doi: https://doi.org/10.1126/science.228.4699.533
Day VW, Klemperer WG. Metal oxide chemistry in solution: the early transition metal polyoxoanions. Science. 1985 May 03;228(4699):533-41. doi: 10.1126/science.228.4699.533. PMID: 17736064.
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Frontiers in electronic structure theory.

The Journal of chemical physics

Sherrill CD.
PMID: 20331271
J Chem Phys. 2010 Mar 21;132(11):110902. doi: 10.1063/1.3369628.

Current and emerging research areas in electronic structure theory promise to greatly extend the scope and quality of quantum chemical computations. Two particularly challenging problems are the accurate description of electronic near-degeneracies (as occur in bond-breaking reactions, first-row transition...

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Sherrill CD. Frontiers in electronic structure theory. J Chem Phys. 2010;132(11):110902doi: 10.1063/1.3369628.
Sherrill, C. D. (2010). Frontiers in electronic structure theory. The Journal of chemical physics, 132(11), 110902. https://doi.org/10.1063/1.3369628
Sherrill, C David. "Frontiers in electronic structure theory." The Journal of chemical physics vol. 132,11 (2010): 110902. doi: https://doi.org/10.1063/1.3369628
Sherrill CD. Frontiers in electronic structure theory. J Chem Phys. 2010 Mar 21;132(11):110902. doi: 10.1063/1.3369628. PMID: 20331271.
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High temperature magnetic ordering in the 4d perovskite SrTcO3.

Physical review letters

Rodriguez EE, Poineau F, Llobet A, Kennedy BJ, Avdeev M, Thorogood GJ, Carter ML, Seshadri R, Singh DJ, Cheetham AK.
PMID: 21405490
Phys Rev Lett. 2011 Feb 11;106(6):067201. doi: 10.1103/PhysRevLett.106.067201. Epub 2011 Feb 07.

We present evidence for possibly the highest magnetic ordering temperature in any compound without 3d transition elements. Neutron powder diffraction measurements, at both time-of-flight and constant wavelength sources, were performed on two independently prepared SrTcO3 powders. SrTcO3 adopts a...

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Rodriguez EE, Poineau F, Llobet A, et al. High temperature magnetic ordering in the 4d perovskite SrTcO3. Phys Rev Lett. 2011;106(6):067201doi: 10.1103/PhysRevLett.106.067201.
Rodriguez, E. E., Poineau, F., Llobet, A., Kennedy, B. J., Avdeev, M., Thorogood, G. J., Carter, M. L., Seshadri, R., Singh, D. J., & Cheetham, A. K. (2011). High temperature magnetic ordering in the 4d perovskite SrTcO3. Physical review letters, 106(6), 067201. https://doi.org/10.1103/PhysRevLett.106.067201
Rodriguez, Efrain E, et al. "High temperature magnetic ordering in the 4d perovskite SrTcO3." Physical review letters vol. 106,6 (2011): 067201. doi: https://doi.org/10.1103/PhysRevLett.106.067201
Rodriguez EE, Poineau F, Llobet A, Kennedy BJ, Avdeev M, Thorogood GJ, Carter ML, Seshadri R, Singh DJ, Cheetham AK. High temperature magnetic ordering in the 4d perovskite SrTcO3. Phys Rev Lett. 2011 Feb 11;106(6):067201. doi: 10.1103/PhysRevLett.106.067201. Epub 2011 Feb 07. PMID: 21405490.
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Luminescent heteropolynuclear complexes of 3,5-dimethylpyrazolate [Pt2Au2M2(Me2pz)8] (M = Ag, Cu) showing the synergistic effect of three transition elements in the excited state.

Chemistry (Weinheim an der Bergstrasse, Germany)

Umakoshi K, Saito K, Arikawa Y, Onishi M, Ishizaka S, Kitamura N, Nakao Y, Sakaki S.
PMID: 19283817
Chemistry. 2009;15(17):4238-42. doi: 10.1002/chem.200900290.

Swap the coins! The Pt(2)Au(2), Pt(2)Au(2)Cu(2), and Pt(2)Au(2)Ag(2) complexes of 3,5-dimethylpyrazolate exhibit yellow-green, orange, and sky-blue luminescence, respectively (see figure). The emission energies of Pt(2)Au(2)M(2) complexes can be controlled by the change of the third coinage metal ions M....

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Umakoshi K, Saito K, Arikawa Y, et al. Luminescent heteropolynuclear complexes of 3,5-dimethylpyrazolate [Pt2Au2M2(Me2pz)8] (M = Ag, Cu) showing the synergistic effect of three transition elements in the excited state. Chemistry. 2009;15(17):4238-42doi: 10.1002/chem.200900290.
Umakoshi, K., Saito, K., Arikawa, Y., Onishi, M., Ishizaka, S., Kitamura, N., Nakao, Y., & Sakaki, S. (2009). Luminescent heteropolynuclear complexes of 3,5-dimethylpyrazolate [Pt2Au2M2(Me2pz)8] (M = Ag, Cu) showing the synergistic effect of three transition elements in the excited state. Chemistry (Weinheim an der Bergstrasse, Germany), 15(17), 4238-42. https://doi.org/10.1002/chem.200900290
Umakoshi, Keisuke, et al. "Luminescent heteropolynuclear complexes of 3,5-dimethylpyrazolate [Pt2Au2M2(Me2pz)8] (M = Ag, Cu) showing the synergistic effect of three transition elements in the excited state." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 15,17 (2009): 4238-42. doi: https://doi.org/10.1002/chem.200900290
Umakoshi K, Saito K, Arikawa Y, Onishi M, Ishizaka S, Kitamura N, Nakao Y, Sakaki S. Luminescent heteropolynuclear complexes of 3,5-dimethylpyrazolate [Pt2Au2M2(Me2pz)8] (M = Ag, Cu) showing the synergistic effect of three transition elements in the excited state. Chemistry. 2009;15(17):4238-42. doi: 10.1002/chem.200900290. PMID: 19283817.
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Showing 1 to 12 of 112 entries