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A new route for generation of alpha-lambda3-iodanyl ketones via ester exchange of (Z)-(beta-acetoxyvinyl)-lambda3-iodanes: their nucleophilic substitutions with halides and sulfur and phosphorus nucleophiles.

The Journal of organic chemistry

Ochiai M, Nishitani J, Nishi Y.
PMID: 12076135
J Org Chem. 2002 Jun 28;67(13):4407-13. doi: 10.1021/jo0107711.

An efficient method for generation of alpha-lambda3-iodanyl ketones from (Z)-(2-acetoxyvinyl)(phenyl)-lambda3-iodanes was developed. The method involves ester exchange of (Z)-2-acetoxyvinyl-lambda3-iodanes with methanol in the presence of triethylamine. alpha-lambda3-Iodanyl ketones react with a variety of nucleophiles such as halides, thiols, phosphines,...

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Ochiai M, Nishitani J, Nishi Y. A new route for generation of alpha-lambda3-iodanyl ketones via ester exchange of (Z)-(beta-acetoxyvinyl)-lambda3-iodanes: their nucleophilic substitutions with halides and sulfur and phosphorus nucleophiles. J Org Chem. 2002;67(13):4407-13doi: 10.1021/jo0107711.
Ochiai, M., Nishitani, J., & Nishi, Y. (2002). A new route for generation of alpha-lambda3-iodanyl ketones via ester exchange of (Z)-(beta-acetoxyvinyl)-lambda3-iodanes: their nucleophilic substitutions with halides and sulfur and phosphorus nucleophiles. The Journal of organic chemistry, 67(13), 4407-13. https://doi.org/10.1021/jo0107711
Ochiai, Masahito, et al. "A new route for generation of alpha-lambda3-iodanyl ketones via ester exchange of (Z)-(beta-acetoxyvinyl)-lambda3-iodanes: their nucleophilic substitutions with halides and sulfur and phosphorus nucleophiles." The Journal of organic chemistry vol. 67,13 (2002): 4407-13. doi: https://doi.org/10.1021/jo0107711
Ochiai M, Nishitani J, Nishi Y. A new route for generation of alpha-lambda3-iodanyl ketones via ester exchange of (Z)-(beta-acetoxyvinyl)-lambda3-iodanes: their nucleophilic substitutions with halides and sulfur and phosphorus nucleophiles. J Org Chem. 2002 Jun 28;67(13):4407-13. doi: 10.1021/jo0107711. PMID: 12076135.
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Iron-Semiquinone, Semiquinone-Semiquinone, and Iron-Iron Magnetic Exchange in Monomeric and Dimeric Ferric Complexes Containing the 3,6-Di-tert-butyl-1,2-semiquinonate Ligand.

Inorganic chemistry

Attia AS, Conklin BJ, Lange CW, Pierpont CG.
PMID: 11666281
Inorg Chem. 1996 Feb 14;35(4):1033-1038. doi: 10.1021/ic950595c.

Fe(3,6-DBSQ)(3) has been prepared by reacting 3,6-di-tert-butyl-1,2-benzoquinone with Fe(CO)(5). The complex has been characterized structurally [orthorhombic, Pbca, a = 18.277(5) Å, b = 11.634(3) Å, c = 39.903(10) Å, V = 8485(4) Å(3), Z = 8, R = 0.063],...

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Attia AS, Conklin BJ, Lange CW, et al. Iron-Semiquinone, Semiquinone-Semiquinone, and Iron-Iron Magnetic Exchange in Monomeric and Dimeric Ferric Complexes Containing the 3,6-Di-tert-butyl-1,2-semiquinonate Ligand. Inorg Chem. 1996;35(4):1033-1038doi: 10.1021/ic950595c.
Attia, A. S., Conklin, B. J., Lange, C. W., & Pierpont, C. G. (1996). Iron-Semiquinone, Semiquinone-Semiquinone, and Iron-Iron Magnetic Exchange in Monomeric and Dimeric Ferric Complexes Containing the 3,6-Di-tert-butyl-1,2-semiquinonate Ligand. Inorganic chemistry, 35(4), 1033-1038. https://doi.org/10.1021/ic950595c
Attia, Attia S., et al. "Iron-Semiquinone, Semiquinone-Semiquinone, and Iron-Iron Magnetic Exchange in Monomeric and Dimeric Ferric Complexes Containing the 3,6-Di-tert-butyl-1,2-semiquinonate Ligand." Inorganic chemistry vol. 35,4 (1996): 1033-1038. doi: https://doi.org/10.1021/ic950595c
Attia AS, Conklin BJ, Lange CW, Pierpont CG. Iron-Semiquinone, Semiquinone-Semiquinone, and Iron-Iron Magnetic Exchange in Monomeric and Dimeric Ferric Complexes Containing the 3,6-Di-tert-butyl-1,2-semiquinonate Ligand. Inorg Chem. 1996 Feb 14;35(4):1033-1038. doi: 10.1021/ic950595c. PMID: 11666281.
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Effects of liquid phase composition on salt cluster formation in positive ion mode electrospray mass spectrometry: implications for clustering mechanism in electrospray.

Journal of the American Society for Mass Spectrometry

Charles L, Pépin D, Gonnet F, Tabet JC.
PMID: 11605968
J Am Soc Mass Spectrom. 2001 Oct;12(10):1077-84. doi: 10.1016/S1044-0305(01)00290-2.

Potassium bromate salt clusters, [KBrO3]nKx(x+), formed by electrospray ionization were studied as a function of solution properties. Clusters with up to 4 positive charges were observed. Their abundance, charge state and distribution were shown to vary with the organic...

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Charles L, Pépin D, Gonnet F, et al. Effects of liquid phase composition on salt cluster formation in positive ion mode electrospray mass spectrometry: implications for clustering mechanism in electrospray. J Am Soc Mass Spectrom. 2001;12(10):1077-84doi: 10.1016/S1044-0305(01)00290-2.
Charles, L., Pépin, D., Gonnet, F., & Tabet, J. C. (2001). Effects of liquid phase composition on salt cluster formation in positive ion mode electrospray mass spectrometry: implications for clustering mechanism in electrospray. Journal of the American Society for Mass Spectrometry, 12(10), 1077-84. https://doi.org/10.1016/S1044-0305(01)00290-2
Charles, L, et al. "Effects of liquid phase composition on salt cluster formation in positive ion mode electrospray mass spectrometry: implications for clustering mechanism in electrospray." Journal of the American Society for Mass Spectrometry vol. 12,10 (2001): 1077-84. doi: https://doi.org/10.1016/S1044-0305(01)00290-2
Charles L, Pépin D, Gonnet F, Tabet JC. Effects of liquid phase composition on salt cluster formation in positive ion mode electrospray mass spectrometry: implications for clustering mechanism in electrospray. J Am Soc Mass Spectrom. 2001 Oct;12(10):1077-84. doi: 10.1016/S1044-0305(01)00290-2. PMID: 11605968.
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Reaction Mechanism for Olefin Exchange at Chloro Ethene Complexes of Platinum(II).

Inorganic chemistry

Plutino MR, Otto S, Roodt A, Elding LI.
PMID: 11670907
Inorg Chem. 1999 Mar 22;38(6):1233-1238. doi: 10.1021/ic981020t.

Complex equilibria in methanol/chloroform/dichloromethane solutions containing Zeise's anion, [PtCl(3)(C(2)H(4))](-) (1), the solvento species, trans-[PtCl(2)(C(2)H(4))(MeOH)] (2), and the dinuclear complex, trans-[PtCl(2)(C(2)H(4))](2) (3), have been studied by UV-vis, (1)H, and (195)Pt NMR spectroscopy, giving average values of K(Cl) = (1.6 +/-...

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Plutino MR, Otto S, Roodt A, et al. Reaction Mechanism for Olefin Exchange at Chloro Ethene Complexes of Platinum(II). Inorg Chem. 1999;38(6):1233-1238doi: 10.1021/ic981020t.
Plutino, M. R., Otto, S., Roodt, A., & Elding, L. I. (1999). Reaction Mechanism for Olefin Exchange at Chloro Ethene Complexes of Platinum(II). Inorganic chemistry, 38(6), 1233-1238. https://doi.org/10.1021/ic981020t
Plutino, Maria Rosaria, et al. "Reaction Mechanism for Olefin Exchange at Chloro Ethene Complexes of Platinum(II)." Inorganic chemistry vol. 38,6 (1999): 1233-1238. doi: https://doi.org/10.1021/ic981020t
Plutino MR, Otto S, Roodt A, Elding LI. Reaction Mechanism for Olefin Exchange at Chloro Ethene Complexes of Platinum(II). Inorg Chem. 1999 Mar 22;38(6):1233-1238. doi: 10.1021/ic981020t. PMID: 11670907.
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Encapsulation of N(2), O(2), methanol, or acetonitrile by decamethylcucurbit[5]uril(NH(4)(+))(2) complexes in the gas phase: influence of the guest on "lid" tightness.

Journal of the American Chemical Society

Kellersberger KA, Anderson JD, Ward SM, Krakowiak KE, Dearden DV.
PMID: 11697985
J Am Chem Soc. 2001 Nov 14;123(45):11316-7. doi: 10.1021/ja017031u.

No abstract available.

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Kellersberger KA, Anderson JD, Ward SM, et al. Encapsulation of N(2), O(2), methanol, or acetonitrile by decamethylcucurbit[5]uril(NH(4)(+))(2) complexes in the gas phase: influence of the guest on "lid" tightness. J Am Chem Soc. 2001;123(45):11316-7doi: 10.1021/ja017031u.
Kellersberger, K. A., Anderson, J. D., Ward, S. M., Krakowiak, K. E., & Dearden, D. V. (2001). Encapsulation of N(2), O(2), methanol, or acetonitrile by decamethylcucurbit[5]uril(NH(4)(+))(2) complexes in the gas phase: influence of the guest on "lid" tightness. Journal of the American Chemical Society, 123(45), 11316-7. https://doi.org/10.1021/ja017031u
Kellersberger, K A, et al. "Encapsulation of N(2), O(2), methanol, or acetonitrile by decamethylcucurbit[5]uril(NH(4)(+))(2) complexes in the gas phase: influence of the guest on "lid" tightness." Journal of the American Chemical Society vol. 123,45 (2001): 11316-7. doi: https://doi.org/10.1021/ja017031u
Kellersberger KA, Anderson JD, Ward SM, Krakowiak KE, Dearden DV. Encapsulation of N(2), O(2), methanol, or acetonitrile by decamethylcucurbit[5]uril(NH(4)(+))(2) complexes in the gas phase: influence of the guest on "lid" tightness. J Am Chem Soc. 2001 Nov 14;123(45):11316-7. doi: 10.1021/ja017031u. PMID: 11697985.
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A New Coupling Reaction of Alkyl Iodides with Electron Deficient Alkenes Using Nickel Boride (cat.)-Borohydride Exchange Resin in Methanol.

The Journal of organic chemistry

Sim TB, Choi J, Joung MJ, Yoon NM.
PMID: 11671567
J Org Chem. 1997 Apr 18;62(8):2357-2361. doi: 10.1021/jo961751f.

The radical addition reaction of alkyl iodides with alpha,beta-unsaturated esters, nitriles, and ketones proceeds in moderate to excellent yields (50-95%) using Ni(OAc)(2) (0.05-0.2 equiv)-BER (3-5 equiv) in methanol in 1-9 h at room temperature or at 65 degrees C....

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Sim TB, Choi J, Joung MJ, et al. A New Coupling Reaction of Alkyl Iodides with Electron Deficient Alkenes Using Nickel Boride (cat.)-Borohydride Exchange Resin in Methanol. J Org Chem. 1997;62(8):2357-2361doi: 10.1021/jo961751f.
Sim, T. B., Choi, J., Joung, M. J., & Yoon, N. M. (1997). A New Coupling Reaction of Alkyl Iodides with Electron Deficient Alkenes Using Nickel Boride (cat.)-Borohydride Exchange Resin in Methanol. The Journal of organic chemistry, 62(8), 2357-2361. https://doi.org/10.1021/jo961751f
Sim, Tae Bo, et al. "A New Coupling Reaction of Alkyl Iodides with Electron Deficient Alkenes Using Nickel Boride (cat.)-Borohydride Exchange Resin in Methanol." The Journal of organic chemistry vol. 62,8 (1997): 2357-2361. doi: https://doi.org/10.1021/jo961751f
Sim TB, Choi J, Joung MJ, Yoon NM. A New Coupling Reaction of Alkyl Iodides with Electron Deficient Alkenes Using Nickel Boride (cat.)-Borohydride Exchange Resin in Methanol. J Org Chem. 1997 Apr 18;62(8):2357-2361. doi: 10.1021/jo961751f. PMID: 11671567.
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New diphosphine ligands containing ethyleneglycol and amino alcohol spacers for the rhodium-catalyzed carbonylation of methanol.

Chemistry (Weinheim an der Bergstrasse, Germany)

Thomas CM, Mafua R, Therrien B, Rusanov E, Stoeckli-Evans H, Süss-Fink G.
PMID: 12203315
Chemistry. 2002 Aug 02;8(15):3343-52. doi: 10.1002/1521-3765(20020802)8:15<3343::AID-CHEM3343>3.0.CO;2-Z.

The new diphosphine ligands Ph(2)PC(6)H(4)C(O)X(CH(2))(2)OC(O)C(6)H(4)PPh(2) (1: X=NH; 2: X=NPh; 3: X=O) and Ph(2)PC(6)H(4)C(O)O(CH(2))(2)O(CH(2))(2)OC(O)C(6)H(4)PPh(2) (5) as well as the monophosphine ligand Ph(2)PC(6)H(4)C(O)X(CH(2))(2)OH (4) have been prepared from 2-diphenylphosphinobenzoic acid and the corresponding amino alcohols or diols. Coordination of the diphosphine...

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Thomas CM, Mafua R, Therrien B, et al. New diphosphine ligands containing ethyleneglycol and amino alcohol spacers for the rhodium-catalyzed carbonylation of methanol. Chemistry. 2002;8(15):3343-52doi: 10.1002/1521-3765(20020802)8:15<3343::AID-CHEM3343>3.0.CO;2-Z.
Thomas, C. M., Mafua, R., Therrien, B., Rusanov, E., Stoeckli-Evans, H., & Süss-Fink, G. (2002). New diphosphine ligands containing ethyleneglycol and amino alcohol spacers for the rhodium-catalyzed carbonylation of methanol. Chemistry (Weinheim an der Bergstrasse, Germany), 8(15), 3343-52. https://doi.org/10.1002/1521-3765(20020802)8:15<3343::AID-CHEM3343>3.0.CO;2-Z
Thomas, Christophe M, et al. "New diphosphine ligands containing ethyleneglycol and amino alcohol spacers for the rhodium-catalyzed carbonylation of methanol." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 8,15 (2002): 3343-52. doi: https://doi.org/10.1002/1521-3765(20020802)8:15<3343::AID-CHEM3343>3.0.CO;2-Z
Thomas CM, Mafua R, Therrien B, Rusanov E, Stoeckli-Evans H, Süss-Fink G. New diphosphine ligands containing ethyleneglycol and amino alcohol spacers for the rhodium-catalyzed carbonylation of methanol. Chemistry. 2002 Aug 02;8(15):3343-52. doi: 10.1002/1521-3765(20020802)8:15<3343::AID-CHEM3343>3.0.CO;2-Z. PMID: 12203315.
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Selective adduct formation by furan chemical ionization reagent in gas chromatography ion trap mass spectrometry.

Journal of mass spectrometry : JMS

Tzing SH, Ghule A, Chang JY, Ling YC.
PMID: 12717752
J Mass Spectrom. 2003 Apr;38(4):401-8. doi: 10.1002/jms.452.

The analytical potential of furan as a chemical ionization (CI) reagent was evaluated for selectivity with nine monosubstituted naphthalene compounds. The ion-molecule reactions of furan and tetrahydrofuran (THF) were compared with those of methane, methanol and acetonitrile (prominently producing...

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Tzing SH, Ghule A, Chang JY, et al. Selective adduct formation by furan chemical ionization reagent in gas chromatography ion trap mass spectrometry. J Mass Spectrom. 2003;38(4):401-8doi: 10.1002/jms.452.
Tzing, S. H., Ghule, A., Chang, J. Y., & Ling, Y. C. (2003). Selective adduct formation by furan chemical ionization reagent in gas chromatography ion trap mass spectrometry. Journal of mass spectrometry : JMS, 38(4), 401-8. https://doi.org/10.1002/jms.452
Tzing, Shin-Hwa, et al. "Selective adduct formation by furan chemical ionization reagent in gas chromatography ion trap mass spectrometry." Journal of mass spectrometry : JMS vol. 38,4 (2003): 401-8. doi: https://doi.org/10.1002/jms.452
Tzing SH, Ghule A, Chang JY, Ling YC. Selective adduct formation by furan chemical ionization reagent in gas chromatography ion trap mass spectrometry. J Mass Spectrom. 2003 Apr;38(4):401-8. doi: 10.1002/jms.452. PMID: 12717752.
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Solvent switching of intramolecular energy transfer in bichromophoric systems: photophysics of (2,2'-bipyridine)tetracyanoruthenate(II)/pyrenyl complexes.

Inorganic chemistry

Indelli MT, Ghirotti M, Prodi A, Chiorboli C, Scandola F, McClenaghan ND, Puntoriero F, Campagna S.
PMID: 12950195
Inorg Chem. 2003 Sep 08;42(18):5489-97. doi: 10.1021/ic034185x.

The supramolecular systems [Ru(Pyr(n)bpy)(CN)(4)](2-) (n = 1, 2), where one and two pyrenyl units are linked via two-methylene bridges to the [Ru(bpy)(CN)(4)](2-) chromophore, have been synthesized. The photophysical properties of these systems, which contain a highly solvatochromic metal complex...

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Indelli MT, Ghirotti M, Prodi A, et al. Solvent switching of intramolecular energy transfer in bichromophoric systems: photophysics of (2,2'-bipyridine)tetracyanoruthenate(II)/pyrenyl complexes. Inorg Chem. 2003;42(18):5489-97doi: 10.1021/ic034185x.
Indelli, M. T., Ghirotti, M., Prodi, A., Chiorboli, C., Scandola, F., McClenaghan, N. D., Puntoriero, F., & Campagna, S. (2003). Solvent switching of intramolecular energy transfer in bichromophoric systems: photophysics of (2,2'-bipyridine)tetracyanoruthenate(II)/pyrenyl complexes. Inorganic chemistry, 42(18), 5489-97. https://doi.org/10.1021/ic034185x
Indelli, M T, et al. "Solvent switching of intramolecular energy transfer in bichromophoric systems: photophysics of (2,2'-bipyridine)tetracyanoruthenate(II)/pyrenyl complexes." Inorganic chemistry vol. 42,18 (2003): 5489-97. doi: https://doi.org/10.1021/ic034185x
Indelli MT, Ghirotti M, Prodi A, Chiorboli C, Scandola F, McClenaghan ND, Puntoriero F, Campagna S. Solvent switching of intramolecular energy transfer in bichromophoric systems: photophysics of (2,2'-bipyridine)tetracyanoruthenate(II)/pyrenyl complexes. Inorg Chem. 2003 Sep 08;42(18):5489-97. doi: 10.1021/ic034185x. PMID: 12950195.
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New chloro, mu-oxo, and alkyl derivatives of dioxomolybdenum(VI) and -tungsten(VI) complexes chelated with N(2)O tridentate ligands: synthesis and catalytic activities toward olefin epoxidation.

Inorganic chemistry

Wong YL, Ng DK, Lee HK.
PMID: 12354062
Inorg Chem. 2002 Oct 07;41(20):5276-85. doi: 10.1021/ic020173k.

A new series of cis-dioxomolybdenum(VI) complexes MoO(2)(L(n))Cl (n = 1-5) were prepared by the reaction of MoO(2)Cl(2)(DME) (DME = 1,2-dimethoxyethane) with 2-N-(2-pyridylmethyl)aminophenol (HL(1)) or its N-alkyl derivatives (HL(n)) (n = 2-5) in the presence of triethylamine. The new mu-oxo...

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Wong YL, Ng DK, Lee HK. New chloro, mu-oxo, and alkyl derivatives of dioxomolybdenum(VI) and -tungsten(VI) complexes chelated with N(2)O tridentate ligands: synthesis and catalytic activities toward olefin epoxidation. Inorg Chem. 2002;41(20):5276-85doi: 10.1021/ic020173k.
Wong, Y. L., Ng, D. K., & Lee, H. K. (2002). New chloro, mu-oxo, and alkyl derivatives of dioxomolybdenum(VI) and -tungsten(VI) complexes chelated with N(2)O tridentate ligands: synthesis and catalytic activities toward olefin epoxidation. Inorganic chemistry, 41(20), 5276-85. https://doi.org/10.1021/ic020173k
Wong, Yee-Lok, et al. "New chloro, mu-oxo, and alkyl derivatives of dioxomolybdenum(VI) and -tungsten(VI) complexes chelated with N(2)O tridentate ligands: synthesis and catalytic activities toward olefin epoxidation." Inorganic chemistry vol. 41,20 (2002): 5276-85. doi: https://doi.org/10.1021/ic020173k
Wong YL, Ng DK, Lee HK. New chloro, mu-oxo, and alkyl derivatives of dioxomolybdenum(VI) and -tungsten(VI) complexes chelated with N(2)O tridentate ligands: synthesis and catalytic activities toward olefin epoxidation. Inorg Chem. 2002 Oct 07;41(20):5276-85. doi: 10.1021/ic020173k. PMID: 12354062.
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meso-5,5,7,12,12,14-Hexamethyl-4,11-diaza-1,8-diazoniacyclotetradecane (S)-malate(2-) methanol disolvate: a chain of rings generated by two pairs of N-H.O hydrogen bonds.

Acta crystallographica. Section C, Crystal structure communications

Bowes KF, Ferguson G, Lough AJ, Glidewell C.
PMID: 12794354
Acta Crystallogr C. 2003 Jun;59:o329-31. doi: 10.1107/s010827010300920x. Epub 2003 May 20.

The title compound is a methanol-solvated salt, C(16)H(38)N(4)(2+).C(4)H(4)O(5)(2-).2CH(3)OH, in which the ionic components are linked into chains by two pairs of N-H.O hydrogen bonds [H.O = 1.78-2.21 A, N.O = 2.702 (14)-3.094 (8) A and N-H.O = 160-179 degrees...

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Bowes KF, Ferguson G, Lough AJ, et al. meso-5,5,7,12,12,14-Hexamethyl-4,11-diaza-1,8-diazoniacyclotetradecane (S)-malate(2-) methanol disolvate: a chain of rings generated by two pairs of N-H.O hydrogen bonds. Acta Crystallogr C. 2003;59:o329-31doi: 10.1107/s010827010300920x.
Bowes, K. F., Ferguson, G., Lough, A. J., & Glidewell, C. (2003). meso-5,5,7,12,12,14-Hexamethyl-4,11-diaza-1,8-diazoniacyclotetradecane (S)-malate(2-) methanol disolvate: a chain of rings generated by two pairs of N-H.O hydrogen bonds. Acta crystallographica. Section C, Crystal structure communications, 59o329-31. https://doi.org/10.1107/s010827010300920x
Bowes, Katharine F, et al. "meso-5,5,7,12,12,14-Hexamethyl-4,11-diaza-1,8-diazoniacyclotetradecane (S)-malate(2-) methanol disolvate: a chain of rings generated by two pairs of N-H.O hydrogen bonds." Acta crystallographica. Section C, Crystal structure communications vol. 59 (2003): o329-31. doi: https://doi.org/10.1107/s010827010300920x
Bowes KF, Ferguson G, Lough AJ, Glidewell C. meso-5,5,7,12,12,14-Hexamethyl-4,11-diaza-1,8-diazoniacyclotetradecane (S)-malate(2-) methanol disolvate: a chain of rings generated by two pairs of N-H.O hydrogen bonds. Acta Crystallogr C. 2003 Jun;59:o329-31. doi: 10.1107/s010827010300920x. Epub 2003 May 20. PMID: 12794354.
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Steric and electronic effects on the reactivity of rh and ir complexes containing P-S, P-P, and P-O ligands. Implications for the effects of chelate ligands in catalysis.

Journal of the American Chemical Society

Gonsalvi L, Adams H, Sunley GJ, Ditzel E, Haynes A.
PMID: 12418915
J Am Chem Soc. 2002 Nov 13;124(45):13597-612. doi: 10.1021/ja0176191.

Kinetic studies of the reactions of [M(CO)(L-L)I] [M = Rh, Ir; L-L = Ph(2)PCH(2)P(S)Ph(2) (dppms), Ph(2)PCH(2)CH(2)PPh(2) (dppe), and Ph(2)PCH(2)P(O)Ph(2) (dppmo)] with methyl iodide have been undertaken. All the chelate ligands promote oxidative addition of methyl iodide to the square...

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Gonsalvi L, Adams H, Sunley GJ, et al. Steric and electronic effects on the reactivity of rh and ir complexes containing P-S, P-P, and P-O ligands. Implications for the effects of chelate ligands in catalysis. J Am Chem Soc. 2002;124(45):13597-612doi: 10.1021/ja0176191.
Gonsalvi, L., Adams, H., Sunley, G. J., Ditzel, E., & Haynes, A. (2002). Steric and electronic effects on the reactivity of rh and ir complexes containing P-S, P-P, and P-O ligands. Implications for the effects of chelate ligands in catalysis. Journal of the American Chemical Society, 124(45), 13597-612. https://doi.org/10.1021/ja0176191
Gonsalvi, Luca, et al. "Steric and electronic effects on the reactivity of rh and ir complexes containing P-S, P-P, and P-O ligands. Implications for the effects of chelate ligands in catalysis." Journal of the American Chemical Society vol. 124,45 (2002): 13597-612. doi: https://doi.org/10.1021/ja0176191
Gonsalvi L, Adams H, Sunley GJ, Ditzel E, Haynes A. Steric and electronic effects on the reactivity of rh and ir complexes containing P-S, P-P, and P-O ligands. Implications for the effects of chelate ligands in catalysis. J Am Chem Soc. 2002 Nov 13;124(45):13597-612. doi: 10.1021/ja0176191. PMID: 12418915.
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