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[Problem of the quality of radiological pictures].

Polski przeglad radiologii i medycyny nuklearnej

Gladysz B.
PMID: 5976724
Pol Przegl Radiol Med Nukl. 1966 Sep-Oct;30(5):561-5.

No abstract available.

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Gladysz B. Zagadnienie jakości obrazu. [Problem of the quality of radiological pictures]. Pol Przegl Radiol Med Nukl. 1966;30(5):561-5
Gladysz, B. (1966). Zagadnienie jakości obrazu. [Problem of the quality of radiological pictures]. Polski przeglad radiologii i medycyny nuklearnej, 30(5), 561-5.
Gladysz, B. "Zagadnienie jakości obrazu." [Problem of the quality of radiological pictures]. Polski przeglad radiologii i medycyny nuklearnej vol. 30,5 (1966): 561-5.
Gladysz B. Zagadnienie jakości obrazu. [Problem of the quality of radiological pictures]. Pol Przegl Radiol Med Nukl. 1966 Sep-Oct;30(5):561-5. Polish. PMID: 5976724.
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Activation of Single-Component Nickel(II) Polyethylene Catalysts via Phase Transfer of Fluorous Phosphine Ligands.

Journal of the American Chemical Society

Xi Z, Bazzi HS, Gladysz JA.
PMID: 26300472
J Am Chem Soc. 2015 Sep 02;137(34):10930-3. doi: 10.1021/jacs.5b06562. Epub 2015 Aug 24.

The nickel salicylaldiminato phosphine complexes [1,2,3-C6H3(9-anthracenyl)O(CH═N(2,6-C6H3(iPr)2)]Ni(Me)[P(4-C6H4R)3] (4; R = a, (CH2)2Rf8; b, (CH2)3Rf8; c, H (Rf8 = (CF2)7CF3)) are prepared from the corresponding phosphines 3a-c and nickel NCMe adduct (46-68%). These are applied as catalysts for ethylene polymerization in...

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Xi Z, Bazzi HS, Gladysz JA. Activation of Single-Component Nickel(II) Polyethylene Catalysts via Phase Transfer of Fluorous Phosphine Ligands. J Am Chem Soc. 2015;137(34):10930-3doi: 10.1021/jacs.5b06562.
Xi, Z., Bazzi, H. S., & Gladysz, J. A. (2015). Activation of Single-Component Nickel(II) Polyethylene Catalysts via Phase Transfer of Fluorous Phosphine Ligands. Journal of the American Chemical Society, 137(34), 10930-3. https://doi.org/10.1021/jacs.5b06562
Xi, Zhenxing, et al. "Activation of Single-Component Nickel(II) Polyethylene Catalysts via Phase Transfer of Fluorous Phosphine Ligands." Journal of the American Chemical Society vol. 137,34 (2015): 10930-3. doi: https://doi.org/10.1021/jacs.5b06562
Xi Z, Bazzi HS, Gladysz JA. Activation of Single-Component Nickel(II) Polyethylene Catalysts via Phase Transfer of Fluorous Phosphine Ligands. J Am Chem Soc. 2015 Sep 02;137(34):10930-3. doi: 10.1021/jacs.5b06562. Epub 2015 Aug 24. PMID: 26300472.
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Octahedral Gyroscope-like Molecules Consisting of Rhenium Rotators within Cage-like Dibridgehead Diphosphine Stators: Syntheses, Substitution Reactions, Structures, and Dynamic Properties.

Inorganic chemistry

Hess GD, Fiedler T, Hampel F, Gladysz JA.
PMID: 28598610
Inorg Chem. 2017 Jul 03;56(13):7454-7469. doi: 10.1021/acs.inorgchem.7b00909. Epub 2017 Jun 09.

Reactions of Re(CO)

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Hess GD, Fiedler T, Hampel F, et al. Octahedral Gyroscope-like Molecules Consisting of Rhenium Rotators within Cage-like Dibridgehead Diphosphine Stators: Syntheses, Substitution Reactions, Structures, and Dynamic Properties. Inorg Chem. 2017;56(13):7454-7469doi: 10.1021/acs.inorgchem.7b00909.
Hess, G. D., Fiedler, T., Hampel, F., & Gladysz, J. A. (2017). Octahedral Gyroscope-like Molecules Consisting of Rhenium Rotators within Cage-like Dibridgehead Diphosphine Stators: Syntheses, Substitution Reactions, Structures, and Dynamic Properties. Inorganic chemistry, 56(13), 7454-7469. https://doi.org/10.1021/acs.inorgchem.7b00909
Hess, Gisela D, et al. "Octahedral Gyroscope-like Molecules Consisting of Rhenium Rotators within Cage-like Dibridgehead Diphosphine Stators: Syntheses, Substitution Reactions, Structures, and Dynamic Properties." Inorganic chemistry vol. 56,13 (2017): 7454-7469. doi: https://doi.org/10.1021/acs.inorgchem.7b00909
Hess GD, Fiedler T, Hampel F, Gladysz JA. Octahedral Gyroscope-like Molecules Consisting of Rhenium Rotators within Cage-like Dibridgehead Diphosphine Stators: Syntheses, Substitution Reactions, Structures, and Dynamic Properties. Inorg Chem. 2017 Jul 03;56(13):7454-7469. doi: 10.1021/acs.inorgchem.7b00909. Epub 2017 Jun 09. PMID: 28598610.
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A Search for pi/sigma Equilibria in Chiral Rhenium Imine Complexes of the Formula [(eta(5)-C(5)H(5))Re(NO)(PPh(3))(N(H)=C(CF(3))X)](+)TfO(-): Investigation of Electronic Effects upon the Binding Mode.

Inorganic chemistry

Stark GA, Gladysz JA.
PMID: 11666738
Inorg Chem. 1996 Sep 11;35(19):5509-5513. doi: 10.1021/ic960302v.

Reaction of the amido complex (eta(5)-C(5)H(5))Re(NO)(PPh(3))(&Numl;H(2)) (2) and hexafluoroacetone gives the methyleneamido complex (eta(5)-C(5)H(5))Re(NO)(PPh(3))(&Numl;=C(CF(3))(2)) (3, 58%). Addition of TfOH to 3 yields the sigma-imine complex [(eta(5)-C(5)H(5))Re(NO)(PPh(3))(eta(1)-N(H)=C(CF(3))(2))](+)TfO(-) (4, 96%). Similar reactions of 2 with trifluoroacetaldehyde and then TfOH give the...

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Stark GA, Gladysz JA. A Search for pi/sigma Equilibria in Chiral Rhenium Imine Complexes of the Formula [(eta(5)-C(5)H(5))Re(NO)(PPh(3))(N(H)=C(CF(3))X)](+)TfO(-): Investigation of Electronic Effects upon the Binding Mode. Inorg Chem. 1996;35(19):5509-5513doi: 10.1021/ic960302v.
Stark, G. A., & Gladysz, J. A. (1996). A Search for pi/sigma Equilibria in Chiral Rhenium Imine Complexes of the Formula [(eta(5)-C(5)H(5))Re(NO)(PPh(3))(N(H)=C(CF(3))X)](+)TfO(-): Investigation of Electronic Effects upon the Binding Mode. Inorganic chemistry, 35(19), 5509-5513. https://doi.org/10.1021/ic960302v
Stark, Gene A., and Gladysz, J. A.. "A Search for pi/sigma Equilibria in Chiral Rhenium Imine Complexes of the Formula [(eta(5)-C(5)H(5))Re(NO)(PPh(3))(N(H)=C(CF(3))X)](+)TfO(-): Investigation of Electronic Effects upon the Binding Mode." Inorganic chemistry vol. 35,19 (1996): 5509-5513. doi: https://doi.org/10.1021/ic960302v
Stark GA, Gladysz JA. A Search for pi/sigma Equilibria in Chiral Rhenium Imine Complexes of the Formula [(eta(5)-C(5)H(5))Re(NO)(PPh(3))(N(H)=C(CF(3))X)](+)TfO(-): Investigation of Electronic Effects upon the Binding Mode. Inorg Chem. 1996 Sep 11;35(19):5509-5513. doi: 10.1021/ic960302v. PMID: 11666738.
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Vibrational progressions in the valence ionizations of transition metal hydrides: evaluation of metal-hydride bonding and vibrations in (eta(5)-C(5)R(5))Re(NO)(CO)H [R = H, CH(3)].

Journal of the American Chemical Society

Lichtenberger DL, Gruhn NE, Rai-Chaudhuri A, Renshaw SK, Gladysz JA, Jiao H, Seyler J, Igau A.
PMID: 11841310
J Am Chem Soc. 2002 Feb 20;124(7):1417-23. doi: 10.1021/ja0120227.

The first examples of vibrational structure in metal-ligand sigma-bond ionizations are observed in the gas-phase photoelectron spectra of CpRe(NO)(CO)H and CpRe(NO)(CO)H [Cp = eta(5)-C(5)H(5), Cp = eta(5)-C(5)(CH(3))(5)]. The vibrational progressions are due to the Re-H stretch in the ion...

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Lichtenberger DL, Gruhn NE, Rai-Chaudhuri A, et al. Vibrational progressions in the valence ionizations of transition metal hydrides: evaluation of metal-hydride bonding and vibrations in (eta(5)-C(5)R(5))Re(NO)(CO)H [R = H, CH(3)]. J Am Chem Soc. 2002;124(7):1417-23doi: 10.1021/ja0120227.
Lichtenberger, D. L., Gruhn, N. E., Rai-Chaudhuri, A., Renshaw, S. K., Gladysz, J. A., Jiao, H., Seyler, J., & Igau, A. (2002). Vibrational progressions in the valence ionizations of transition metal hydrides: evaluation of metal-hydride bonding and vibrations in (eta(5)-C(5)R(5))Re(NO)(CO)H [R = H, CH(3)]. Journal of the American Chemical Society, 124(7), 1417-23. https://doi.org/10.1021/ja0120227
Lichtenberger, Dennis L, et al. "Vibrational progressions in the valence ionizations of transition metal hydrides: evaluation of metal-hydride bonding and vibrations in (eta(5)-C(5)R(5))Re(NO)(CO)H [R = H, CH(3)]." Journal of the American Chemical Society vol. 124,7 (2002): 1417-23. doi: https://doi.org/10.1021/ja0120227
Lichtenberger DL, Gruhn NE, Rai-Chaudhuri A, Renshaw SK, Gladysz JA, Jiao H, Seyler J, Igau A. Vibrational progressions in the valence ionizations of transition metal hydrides: evaluation of metal-hydride bonding and vibrations in (eta(5)-C(5)R(5))Re(NO)(CO)H [R = H, CH(3)]. J Am Chem Soc. 2002 Feb 20;124(7):1417-23. doi: 10.1021/ja0120227. PMID: 11841310.
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How to insulate a reactive site from a perfluoroalkyl group: photoelectron spectroscopy, calorimetric, and computational studies of long-range electronic effects in fluorous phosphines P((CH(2))(m)(CF(2))(7)CF(3))(3).

Journal of the American Chemical Society

Jiao H, Le Stang S, Soós T, Meier R, Kowski K, Rademacher P, Jafarpour L, Hamard JB, Nolan SP, Gladysz JA.
PMID: 11841323
J Am Chem Soc. 2002 Feb 20;124(7):1516-23. doi: 10.1021/ja011877g.

This study advances strategy and design in catalysts and reagents for fluorous and supercritical CO(2) chemistry by defining the structural requirements for insulating a typical active site from a perfluoroalkyl segment. The vertical ionization potentials of the phosphines P((CH(2))(m)R(f8))(3)...

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Jiao H, Le Stang S, Soós T, et al. How to insulate a reactive site from a perfluoroalkyl group: photoelectron spectroscopy, calorimetric, and computational studies of long-range electronic effects in fluorous phosphines P((CH(2))(m)(CF(2))(7)CF(3))(3). J Am Chem Soc. 2002;124(7):1516-23doi: 10.1021/ja011877g.
Jiao, H., Le Stang, S., Soós, T., Meier, R., Kowski, K., Rademacher, P., Jafarpour, L., Hamard, J. B., Nolan, S. P., & Gladysz, J. A. (2002). How to insulate a reactive site from a perfluoroalkyl group: photoelectron spectroscopy, calorimetric, and computational studies of long-range electronic effects in fluorous phosphines P((CH(2))(m)(CF(2))(7)CF(3))(3). Journal of the American Chemical Society, 124(7), 1516-23. https://doi.org/10.1021/ja011877g
Jiao, Haijun, et al. "How to insulate a reactive site from a perfluoroalkyl group: photoelectron spectroscopy, calorimetric, and computational studies of long-range electronic effects in fluorous phosphines P((CH(2))(m)(CF(2))(7)CF(3))(3)." Journal of the American Chemical Society vol. 124,7 (2002): 1516-23. doi: https://doi.org/10.1021/ja011877g
Jiao H, Le Stang S, Soós T, Meier R, Kowski K, Rademacher P, Jafarpour L, Hamard JB, Nolan SP, Gladysz JA. How to insulate a reactive site from a perfluoroalkyl group: photoelectron spectroscopy, calorimetric, and computational studies of long-range electronic effects in fluorous phosphines P((CH(2))(m)(CF(2))(7)CF(3))(3). J Am Chem Soc. 2002 Feb 20;124(7):1516-23. doi: 10.1021/ja011877g. PMID: 11841323.
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Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid phase separation.

Journal of the American Chemical Society

Wende M, Meier R, Gladysz JA.
PMID: 11707132
J Am Chem Soc. 2001 Nov 21;123(46):11490-1. doi: 10.1021/ja011444d.

No abstract available.

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Wende M, Meier R, Gladysz JA. Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid phase separation. J Am Chem Soc. 2001;123(46):11490-1doi: 10.1021/ja011444d.
Wende, M., Meier, R., & Gladysz, J. A. (2001). Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid phase separation. Journal of the American Chemical Society, 123(46), 11490-1. https://doi.org/10.1021/ja011444d
Wende, M, et al. "Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid phase separation." Journal of the American Chemical Society vol. 123,46 (2001): 11490-1. doi: https://doi.org/10.1021/ja011444d
Wende M, Meier R, Gladysz JA. Fluorous catalysis without fluorous solvents: a friendlier catalyst recovery/recycling protocol based upon thermomorphic properties and liquid/solid phase separation. J Am Chem Soc. 2001 Nov 21;123(46):11490-1. doi: 10.1021/ja011444d. PMID: 11707132.
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A new family of chelating diphosphines with a transition metal stereocenter in the backbone: novel applications of "chiral-at-rhenium" complexes in rhodium-catalyzed enantioselective alkene hydrogenations.

Chemistry (Weinheim an der Bergstrasse, Germany)

Kromm K, Zwick BD, Meyer O, Hampel F, Gladysz JA.
PMID: 11405481
Chemistry. 2001 May 04;7(9):2015-27. doi: 10.1002/1521-3765(20010504)7:9<2015::aid-chem2015>3.0.co;2-h.

The title compounds are accessed by sequences starting with racemic and enantiomerically pure [(eta5-C5H5)Re(NO)(PPh3)(CH3)]. Reactions with chlorobenzene/HBF4, PPh2H, and tBuOK give the phosphido complex [(eta5-C5H5)Re(NO)(PPh3)(PPh2)] (3). Reactions with Ph3C+ BF4-, PPh2H, and tBuOK give the methylene homologue [(eta5-C5H5)Re(NO)(PPh3)(CH2PPh2)] (9)....

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Kromm K, Zwick BD, Meyer O, et al. A new family of chelating diphosphines with a transition metal stereocenter in the backbone: novel applications of "chiral-at-rhenium" complexes in rhodium-catalyzed enantioselective alkene hydrogenations. Chemistry. 2001;7(9):2015-27doi: 10.1002/1521-3765(20010504)7:9<2015::aid-chem2015>3.0.co;2-h.
Kromm, K., Zwick, B. D., Meyer, O., Hampel, F., & Gladysz, J. A. (2001). A new family of chelating diphosphines with a transition metal stereocenter in the backbone: novel applications of "chiral-at-rhenium" complexes in rhodium-catalyzed enantioselective alkene hydrogenations. Chemistry (Weinheim an der Bergstrasse, Germany), 7(9), 2015-27. https://doi.org/10.1002/1521-3765(20010504)7:9<2015::aid-chem2015>3.0.co;2-h
Kromm, K, et al. "A new family of chelating diphosphines with a transition metal stereocenter in the backbone: novel applications of "chiral-at-rhenium" complexes in rhodium-catalyzed enantioselective alkene hydrogenations." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 7,9 (2001): 2015-27. doi: https://doi.org/10.1002/1521-3765(20010504)7:9<2015::aid-chem2015>3.0.co;2-h
Kromm K, Zwick BD, Meyer O, Hampel F, Gladysz JA. A new family of chelating diphosphines with a transition metal stereocenter in the backbone: novel applications of "chiral-at-rhenium" complexes in rhodium-catalyzed enantioselective alkene hydrogenations. Chemistry. 2001 May 04;7(9):2015-27. doi: 10.1002/1521-3765(20010504)7:9<2015::aid-chem2015>3.0.co;2-h. PMID: 11405481.
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Synthesis, structure, and reactivity of sp carbon chains with bis(phosphine) pentafluorophenylplatinum endgroups: butadiynediyl (C4) through hexadecaoctaynediyl (C16) bridges, and beyond.

Chemistry (Weinheim an der Bergstrasse, Germany)

Mohr W, Stahl J, Hampel F, Gladysz JA.
PMID: 12866077
Chemistry. 2003 Jul 21;9(14):3324-40. doi: 10.1002/chem.200204741.

The reaction of trans-[(C(6)F(5))(p-tol(3)P)(2)PtCl] (PtCl) and butadiyne (cat. CuI, HNEt(2)) gives trans-[(C(6)F(5))(p-tol(3)P)(2)Pt(Ctbond;C)(2)H] (PtC(4)H, 81 %), which reacts with excess HC(triple bond)CSiEt(3) under Hay coupling conditions (O(2), cat. CuCl/TMEDA, acetone) to yield PtC(6)Si (53 %). A solution of PtC(6)Si in...

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Mohr W, Stahl J, Hampel F, et al. Synthesis, structure, and reactivity of sp carbon chains with bis(phosphine) pentafluorophenylplatinum endgroups: butadiynediyl (C4) through hexadecaoctaynediyl (C16) bridges, and beyond. Chemistry. 2003;9(14):3324-40doi: 10.1002/chem.200204741.
Mohr, W., Stahl, J., Hampel, F., & Gladysz, J. A. (2003). Synthesis, structure, and reactivity of sp carbon chains with bis(phosphine) pentafluorophenylplatinum endgroups: butadiynediyl (C4) through hexadecaoctaynediyl (C16) bridges, and beyond. Chemistry (Weinheim an der Bergstrasse, Germany), 9(14), 3324-40. https://doi.org/10.1002/chem.200204741
Mohr, Wolfgang, et al. "Synthesis, structure, and reactivity of sp carbon chains with bis(phosphine) pentafluorophenylplatinum endgroups: butadiynediyl (C4) through hexadecaoctaynediyl (C16) bridges, and beyond." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 9,14 (2003): 3324-40. doi: https://doi.org/10.1002/chem.200204741
Mohr W, Stahl J, Hampel F, Gladysz JA. Synthesis, structure, and reactivity of sp carbon chains with bis(phosphine) pentafluorophenylplatinum endgroups: butadiynediyl (C4) through hexadecaoctaynediyl (C16) bridges, and beyond. Chemistry. 2003 Jul 21;9(14):3324-40. doi: 10.1002/chem.200204741. PMID: 12866077.
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Synthesis, structure, and reactivity of palladacycles that contain a chiral rhenium fragment in the backbone: New cyclometalation and catalyst design strategies.

Chemistry (Weinheim an der Bergstrasse, Germany)

Friedlein FK, Kromm K, Hampel F, Gladysz JA.
PMID: 16628761
Chemistry. 2006 Jul 05;12(20):5267-81. doi: 10.1002/chem.200501540.

The bromocyclopentadienyl complex [(eta5-C5H4Br)Re(CO)3] is converted to racemic [(eta5-C5H4Br)Re(NO)(PPh3)(CH2PPh2)] (1 b) similarly to a published sequence for cyclopentadienyl analogues. Treatment of enantiopure (S)-[(eta5-C5H5)Re(NO)(PPh3)(CH3)] with nBuLi and I2 gives (S)-[(eta5-C5H4I)Re(NO)(PPh3)(CH3)] ((S)-6 c; 84 %), which is converted (Ph3C+ PF6 -,...

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Friedlein FK, Kromm K, Hampel F, et al. Synthesis, structure, and reactivity of palladacycles that contain a chiral rhenium fragment in the backbone: New cyclometalation and catalyst design strategies. Chemistry. 2006;12(20):5267-81doi: 10.1002/chem.200501540.
Friedlein, F. K., Kromm, K., Hampel, F., & Gladysz, J. A. (2006). Synthesis, structure, and reactivity of palladacycles that contain a chiral rhenium fragment in the backbone: New cyclometalation and catalyst design strategies. Chemistry (Weinheim an der Bergstrasse, Germany), 12(20), 5267-81. https://doi.org/10.1002/chem.200501540
Friedlein, Florian K, et al. "Synthesis, structure, and reactivity of palladacycles that contain a chiral rhenium fragment in the backbone: New cyclometalation and catalyst design strategies." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 12,20 (2006): 5267-81. doi: https://doi.org/10.1002/chem.200501540
Friedlein FK, Kromm K, Hampel F, Gladysz JA. Synthesis, structure, and reactivity of palladacycles that contain a chiral rhenium fragment in the backbone: New cyclometalation and catalyst design strategies. Chemistry. 2006 Jul 05;12(20):5267-81. doi: 10.1002/chem.200501540. PMID: 16628761.
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Fainter and closer: finding planets by symmetry breaking.

Optics express

Ribak EN, Gladysz S.
PMID: 18825194
Opt Express. 2008 Sep 29;16(20):15553-62. doi: 10.1364/oe.16.015553.

Imaging of planets is very difficult, due to the glare from their nearby, much brighter suns. Static and slowly-evolving aberrations are the limiting factors, even after application of adaptive optics. The residual speckle pattern is highly symmetrical due to...

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Ribak EN, Gladysz S. Fainter and closer: finding planets by symmetry breaking. Opt Express. 2008;16(20):15553-62doi: 10.1364/oe.16.015553.
Ribak, E. N., & Gladysz, S. (2008). Fainter and closer: finding planets by symmetry breaking. Optics express, 16(20), 15553-62. https://doi.org/10.1364/oe.16.015553
Ribak, Erez N, and Gladysz, Szymon. "Fainter and closer: finding planets by symmetry breaking." Optics express vol. 16,20 (2008): 15553-62. doi: https://doi.org/10.1364/oe.16.015553
Ribak EN, Gladysz S. Fainter and closer: finding planets by symmetry breaking. Opt Express. 2008 Sep 29;16(20):15553-62. doi: 10.1364/oe.16.015553. PMID: 18825194.
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Electronic structure and chain-length effects in diplatinum polyynediyl complexes trans,trans-[(X)(R3P)2Pt(C triple bond C)(n)Pt(PR3)2(X)]: a computational investigation.

Chemistry (Weinheim an der Bergstrasse, Germany)

Zhuravlev F, Gladysz JA.
PMID: 15540262
Chemistry. 2004 Dec 03;10(24):6510-22. doi: 10.1002/chem.200400643.

Structure and bonding in the title complexes are studied using model compounds trans,trans-[(C6H5)(H3P)2Pt(C triple bond C)(n)Pt(PH3)2(C6H5)] (PtCxPt; x = 2n = 4-26) at the B3LYP/LACVP* level of density functional theory. Conformations in which the platinum square planes are parallel...

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Zhuravlev F, Gladysz JA. Electronic structure and chain-length effects in diplatinum polyynediyl complexes trans,trans-[(X)(R3P)2Pt(C triple bond C)(n)Pt(PR3)2(X)]: a computational investigation. Chemistry. 2004;10(24):6510-22doi: 10.1002/chem.200400643.
Zhuravlev, F., & Gladysz, J. A. (2004). Electronic structure and chain-length effects in diplatinum polyynediyl complexes trans,trans-[(X)(R3P)2Pt(C triple bond C)(n)Pt(PR3)2(X)]: a computational investigation. Chemistry (Weinheim an der Bergstrasse, Germany), 10(24), 6510-22. https://doi.org/10.1002/chem.200400643
Zhuravlev, Fedor, and Gladysz, John A. "Electronic structure and chain-length effects in diplatinum polyynediyl complexes trans,trans-[(X)(R3P)2Pt(C triple bond C)(n)Pt(PR3)2(X)]: a computational investigation." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 10,24 (2004): 6510-22. doi: https://doi.org/10.1002/chem.200400643
Zhuravlev F, Gladysz JA. Electronic structure and chain-length effects in diplatinum polyynediyl complexes trans,trans-[(X)(R3P)2Pt(C triple bond C)(n)Pt(PR3)2(X)]: a computational investigation. Chemistry. 2004 Dec 03;10(24):6510-22. doi: 10.1002/chem.200400643. PMID: 15540262.
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Showing 1 to 12 of 138 entries