Relevant bibliographies by topics / Tetrakis(triphenylphosphine)nickel(0)

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Academic literature on the topic 'Tetrakis(triphenylphosphine)nickel(0)'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Tetrakis(triphenylphosphine)nickel(0)"

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Čermák, Jan, Vratislav Blechta, and Václav Chvalovský. "Cooligomerization of propadiene with propyne catalysed by nickel(0) complexes." Collection of Czechoslovak Chemical Communications 53, no. 6 (1988): 1274–86. http://dx.doi.org/10.1135/cccc19881274.

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Cooligomerization of propadiene with propyne catalysed by bis(1,5-cyclooctadiene)nickel and tetrakis(triphenylphosphine)nickel gives a variety of products, including besides the cooligomers also the homooligomers of both monomers. The type of catalyst affects partially the product distribution due to changes in the degree of oligomerization. Cooligomerization of propadiene with 3-deuteriopropyne provided information about relative proportion of propadiene and propyne units in the oligomers.
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Ramaotsoa, G. Valerie, Ian Strydom, Jenny-Lee Panayides, and Darren Riley. "Immobilized tetrakis(triphenylphosphine)palladium(0) for Suzuki–Miyaura coupling reactions under flow conditions." Reaction Chemistry & Engineering 4, no. 2 (2019): 372–82. http://dx.doi.org/10.1039/c8re00235e.

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An immobilized triphenylphosphine scaffold was prepared by precipitation polymerization and functionalized to afford a cost-effective source of solid-supported tetrakis(triphenylphosphine)palladium(0).
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Avent, Anthony G., F. Goeffrey N. Cloke, Jeremy P. Day, Elaine A. Seddon, Kenneth R. Seddon, and Stephen M. Smedley. "Tetrakis(trimethylphosphine)nickel(0)." Journal of Organometallic Chemistry 341, no. 1-3 (March 1988): 535–41. http://dx.doi.org/10.1016/0022-328x(88)89106-x.

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Crayston, J. A., and G. Davidson. "Vibrational spectroscope of complexes of platinum(0)—I. Tetrakis(triphenylphosphine)platinum(0) and Dioxygenbis(triphenylphosphine)platinum(0)." Spectrochimica Acta Part A: Molecular Spectroscopy 42, no. 11 (January 1986): 1311–16. http://dx.doi.org/10.1016/0584-8539(86)80232-x.

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Zhou, Qi-Lin, and Yao-Zeng Huang. "Direct fluoroalkylation of aromatic compounds catalyzed by tetrakis(triphenylphosphine)nickel." Journal of Fluorine Chemistry 43, no. 3 (June 1989): 385–92. http://dx.doi.org/10.1016/s0022-1139(00)82725-6.

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Xu, Jie, and Peter Wipf. "Indole synthesis by palladium-catalyzed tandem allylic isomerization – furan Diels–Alder reaction." Organic & Biomolecular Chemistry 15, no. 34 (2017): 7093–96. http://dx.doi.org/10.1039/c7ob01654a.

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Plinta, Hans-Jürgen, Robert Gereke, Axel Fischer, Peter G. Jones, and Reinhard Schmutzler. "Darstellung und Reaktionen von zweikernigen Platin(II)-Komplexen; Einkristall-Röntgenstrukturanalyse eines Tetrakis(difluorphosphonato)-Palladat(II)-Komplexes / Preparation and Reactions of Binuclear Platinum(II) Complexes. Single Crystal X-Ray Diffraction Study of a Tetrakis(difluorophosphonato)palladate(II) Complex." Zeitschrift für Naturforschung B 48, no. 6 (June 1, 1993): 737–46. http://dx.doi.org/10.1515/znb-1993-0607.

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o-Methylbenzyldifluorophosphite 2 was obtained by the reaction of o-methylbenzyltrimethyl silyl ether 1 with chlorodifluorophosphine PF2Cl. The reaction of 2 with the palladium(II) complex 3 led to the tetrakis(difluorophosphonato)palladate(II) complex 7. The X-ray structure analysis of 7 confirmed the nearly exact square planar structure at the metal atom of the tetrakis(difluorophosphonato)palladate(II) dianion. Minimal deviations from the ideal geometry at palladium and phosphorus are mainly the result of thermal motion or disorder phenomena in the crystal. In the reaction of the platinum(II) complex 8 with chlorodifluorophosphine the binuclear tetrakis(chlorodifluorophosphine)platinum(II)chloro complex 9 was obtained. In acetonitrile, 9 was cleaved to form the mononuclear complex 10. Similar results were obtained in the oxidative addition reactions of the platinum(0) complex 11 with sulfuryl chloride fluoride, 12, sulfuryl fluoride, 13, and phosphorus pentafluoride. Tetrakis-(triphenylphosphine)-μ-dichlorodiplatinum(II) hexafluorophosphate 14 was isolated. In acetonitrile the mononuclear acetonitrile-bis(triphenylphosphine)chloroplatinum(II) hexafluorophosphate complex 15 was isolated.
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Cai, Ming-Zhong, Chun-Yun Peng, Hong Zhao, and Jia-Di Huang. "Stereoselective Synthesis of 1,3-enynylselenides via Palladium-Catalysed Cross Coupling Reactions." Journal of Chemical Research 2002, no. 8 (August 2002): 376–77. http://dx.doi.org/10.3184/030823402103172365.

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( E)-α-Bromovinylselenides undergo a cross coupling reaction with alkynyl Grignard reagents in the presence of tetrakis(triphenylphosphine)palladium(0) in THF at room temperature to afford 1,3-enynylselenides in good yields.
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Cai, Mingzhong, Wenyan Hao, Hong Zhao, and Caisheng Song. "Stereoselective Synthesis of 1,3-Enynylsilanes via Hydromagnesiation Reaction of Alkynylsilanes." Journal of Chemical Research 2003, no. 8 (August 2003): 485–86. http://dx.doi.org/10.3184/030823403103174623.

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Hydromagnesiation of alkynylsilanes gives ( Z)-α-silylvinyl Grignard reagents, which are cross-coupled with alkynyl iodides in the presence of tetrakis(triphenylphosphine)palladium(0) catalyst to afford stereoselectively 1,3-enynylsilanes in good yields.
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Piers, Edward, and Fraser F. Fleming. "Palladium(0)-catalyzed conversion of vinyl trifluoromethanesulfonates into α,β-unsaturated nitriles." Canadian Journal of Chemistry 71, no. 11 (November 1, 1993): 1867–72. http://dx.doi.org/10.1139/v93-234.

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Treatment (benzene, room temperature) of each of the vinyl trifluoromethanesulfonates 16–23 with dry lithium cyanide in the presence of catalytic amounts of tetrakis(triphenylphosphine)palladium(0) and the crown ether 12-crown-4 provides good to excellent yields of the corresponding α,β-unsaturated nitriles 24–31.
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Dissertations / Theses on the topic "Tetrakis(triphenylphosphine)nickel(0)"

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Werhun, Peter. "Nuclear Magnetic Resonance of Low-Receptivity Nuclides: The First Demonstration of 61Ni SSNMR as Applied to Structural and Crystallographic Characterization of Diamagnetic Nickel Complexes." Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/36525.

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Nuclear magnetic resonance (NMR) spectroscopy has proven to be an invaluable tool for the modern chemist, despite being a relatively insensitive spectroscopic technique. However, it is precisely this insensitivity that limits characterization of low-receptivity nuclides, which make up the bulk of transition metal nuclides, in particular. In this work, high-fields were used to collect the first 61Ni solid-state NMR (SSNMR) spectra of diamagnetic nickel compounds, specifically, bis(1,5-cyclooctadiene)nickel(0) (Ni(cod)2), tetrakis(triphenylphosphite)nickel(0) (Ni[P(OPh)3]4), and tetrakis(triphenylphosphine)nickel(0) (Ni(PPh3)4). This was complemented by NMR study of the co-ordinated ligands and 61Ni density functional theory (DFT) computations. 61Ni SSNMR spectra of Ni(cod)2 were used to determine its isotropic chemical shift (δiso = 965 ± 10 ppm), span (Ω = 1700 ± 50 ppm), skew (κ = -0.15 ± 0.05), quadrupolar coupling constant (CQ = 2.0 ± 0.3 MHz), quadrupolar asymmetry parameter (η = 0.5 ± 0.2), and the relative orientation of the chemical shift and EFG tensors. Solution study of Ni(cod)2 saturated in C6D6 yielded a narrow 61Ni signal, and the temperature dependence of δiso(61Ni) was assessed (δiso being 936.5 ppm at 295 K). The solution is proposed as a secondary chemical shift reference for 61Ni NMR in lieu of the extremely toxic Ni(CO)4 primary reference. For Ni[P(OPh)3]4, 61Ni SSNMR was used to infer the presence of two distinct crystallographic sites and establish ranges for δ¬iso in the solid state, as well as an upper bound for CQ (3.5 MHz for both sites). For Ni(PPh3)4, fitting provided a δiso value of 515 ± 10 ppm, Ω of 50 ± 50 ppm, κ of 0.5 ± 0.5, CQ of 0.05 ± 0.01 MHz, and η of 0.0 ± 0.2. Ni(cod)2 was chosen for study as it is a ubiquitous source of nickel(0), used for both further synthesis of nickel(0) compounds and directly as a catalyst. The study of Ni[P(OPh)3]4 and Ni(PPh3)4 demonstrated the utility of 61Ni SSNMR given the lack of a previously reported crystal structure for both and the transient nature of Ni(PPh3)4 in solution. The work begins in Chapter 1 by introducing the interactions fundamental to NMR spectroscopy, before moving on to briefly review the field of transition metal nuclide NMR, the chemistry of nickel (with an emphasis on homogeneous catalysis with nickel(0)), and the literature with respect to nickel NMR up to this point. In Chapter 2, the theory and practice of NMR are explained, including solid-state NMR, as well as the basic principles of density functional theory NMR computations. The specific experimental and computational methods of this work are also introduced. Lastly, in Chapter 3 the results are discussed in the context of the concepts presented and literature reviewed, and highlight the use of 61Ni NMR as a means to gain novel information about the chemistry of the compounds studied.
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Book chapters on the topic "Tetrakis(triphenylphosphine)nickel(0)"

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Schunn, R. A., E. C. Ashby, and J. Dilts. "Tetrakis(triphenylphosphine)nickel(0)." In Inorganic Syntheses, 124–26. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132449.ch24.

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Coulson, D. R., L. C. Satek, and S. O. Grim. "Tetrakis(triphenylphosphine)palladium(0)." In Inorganic Syntheses, 121–24. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132449.ch23.

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Coulson, D. R., L. C. Satek, and S. O. Grim. "Tetrakis(Triphenylphosphine)Palladium(0)." In Inorganic Syntheses, 107–9. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch28.

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Olechowski, J. R., C. G. Mcalister, R. F. Clark, L. J. Todd, and S. A. Buell. "Tetrakis(Triphenylphosphite)Nickel(0)." In Inorganic Syntheses, 181–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132401.ch50.

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Ugo, R., F. Cariati, G. La Monica, and Joseph J. Mrowca. "Tris- and Tetrakis(Triphenylphosphine)-Platinum(0)." In Inorganic Syntheses, 123–26. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch33.

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Meier, Max, Fred Basolo, W. R. Kroll, D. Moy, and M. G. Romanelli. "Tetrakis(triethylphosphite)nickel(0), Palladium(0), and Platinum(0) Complexes." In Inorganic Syntheses, 112–17. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132449.ch21.

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Meier, Max, Fred Basolo, W. R. Kroll, D. Moy, and M. G. Romanelli. "Tetrakis(Triethyl Phosphite)Nickel(0), Palladium(0), and Platinum(0) Complexes." In Inorganic Syntheses, 104–7. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch27.

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Marder, T. B. "Using Tetrakis(triphenylphosphine)platinum(0)." In Boron Compounds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00090.

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Marder, T. B. "Diboration of Alkynes Using Tetrakis(triphenylphosphine)platinum(0)." In Boron Compounds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00096.

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Schatz, J., and M. Seler. "Tetrakis(triphenylphosphine)palladium(0)-Assisted Suzuki Cross Coupling under Basic Conditions." In Fully Unsaturated Small-Ring Heterocycles and Monocyclic Five-Membered Hetarenes with One Heteroatom, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-109-00268.

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