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Journal articles on the topic 'Alkylphosphine'

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Author: Grafiati

Published: 4 June 2021

Last updated: 20 February 2023

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1

Jia, Huiru, Betül Küçüköz, Yongheng Xing, Poulomi Majumdar, Caishun Zhang, Ahmet Karatay, Gul Yaglioglu, Ayhan Elmali, Jianzhang Zhao, and Mustafa Hayvali. "trans-Bis(alkylphosphine) platinum(ii)-alkynyl complexes showing broadband visible light absorption and long-lived triplet excited states." J. Mater. Chem. C 2, no. 45 (2014): 9720–36. http://dx.doi.org/10.1039/c4tc01675k.

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2

Li, Xiwen, Hua Li, Yongye Zhao, Xiaoying Tang, Sufang Ma, Bing Gong, and Minfeng Li. "Facile synthesis of well-defined hydrophilic polyesters as degradable poly(ethylene glycol)-like biomaterials." Polymer Chemistry 6, no. 36 (2015): 6452–56. http://dx.doi.org/10.1039/c5py00762c.

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Highly stable and polymerizable δ-valerolactones bearing oligo(ethylene glycol) methyl ether functionalities are facilely prepared by alkylphosphine catalyzed thiol–ene addition with an exocyclic α,β-unsaturated δ-valerolactone.

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3

Zhang, Wen, Gang Ye, and Jing Chen. "New insights into the uranium adsorption behavior of mesoporous SBA-15 silicas decorated with alkylphosphine oxide ligands." RSC Advances 6, no. 2 (2016): 1210–17. http://dx.doi.org/10.1039/c5ra21636b.

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Alkylphosphine oxide functionalized mesoporous silicas were prepared by co-condensation and further addition reaction with secondary n-propylphosphine oxide and are promising candidates for the preconcentration and adsorption of uranium from acidic aqueous solutions.

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4

Kendall, Alexander J., Daniel T. Seidenkranz, and David R. Tyler. "Improved Synthetic Route to Heteroleptic Alkylphosphine Oxides." Organometallics 36, no. 13 (June 21, 2017): 2412–17. http://dx.doi.org/10.1021/acs.organomet.7b00304.

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5

Fang, Ji-Ping, Klaus-Dieter Wantke, and Klaus Lunkenheimer. "Evaluation of the Dynamic Surface Tension of Alkylphosphine Oxides." Journal of Physical Chemistry 99, no. 13 (March 1995): 4632–38. http://dx.doi.org/10.1021/j100013a038.

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6

Mimeau, David, Olivier Delacroix, Benoit Join, and Annie-Claude Gaumont. "Easy access to alkylphosphine boranes starting from unactivated alkenes." Comptes Rendus Chimie 7, no. 8-9 (August 2004): 845–54. http://dx.doi.org/10.1016/j.crci.2004.02.016.

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7

Ferrari, M., L. Liggieri, F. Ravera, C. Amodio, and R. Miller. "Adsorption Kinetics of Alkylphosphine Oxides at Water/Hexane Interface." Journal of Colloid and Interface Science 186, no. 1 (February 1997): 40–45. http://dx.doi.org/10.1006/jcis.1996.4579.

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8

Liggieri, L., F. Ravera, M. Ferrari, A. Passerone, and R. Miller. "Adsorption Kinetics of Alkylphosphine Oxides at Water/Hexane Interface." Journal of Colloid and Interface Science 186, no. 1 (February 1997): 46–52. http://dx.doi.org/10.1006/jcis.1996.4580.

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9

Jansen, Achim, and Stephan Pitter. "Synthese hemilabiler P,N-Liganden: x-2-Pyridyl-n-alkylphosphine." Monatshefte fuer Chemie/Chemical Monthly 130, no. 6 (1999): 783. http://dx.doi.org/10.1007/s007060050239.

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10

Kim, Dae-Jin, Ju-Hyun Lee, Jae-Woong Yu, Eui Jung Kim, and Kee-Kahb Koo. "Low temperature non-alkylphosphine based synthesis of cadmium selenide nanocrystals." Colloids and Surfaces A: Physicochemical and Engineering Aspects 313-314 (February 2008): 211–15. http://dx.doi.org/10.1016/j.colsurfa.2007.04.096.

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11

Ito, Shingo, Kagehiro Munakata, Akifumi Nakamura, and Kyoko Nozaki. "Copolymerization of Vinyl Acetate with Ethylene by Palladium/Alkylphosphine−Sulfonate Catalysts." Journal of the American Chemical Society 131, no. 41 (October 21, 2009): 14606–7. http://dx.doi.org/10.1021/ja9050839.

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12

Ricci, Giovanni, Alessandra Forni, Aldo Boglia, and Tiziano Motta. "Synthesis, structure, and butadiene polymerization behavior of alkylphosphine cobalt(II) complexes." Journal of Molecular Catalysis A: Chemical 226, no. 2 (February 2005): 235–41. http://dx.doi.org/10.1016/j.molcata.2004.10.022.

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13

Ropartz, Loïc, Douglas F. Foster, Russell E. Morris, Alexandra M. Z. Slawin, and David J. Cole-Hamilton. "Hydrocarbonylation reactions using alkylphosphine-containing dendrimers based on a polyhedral oligosilsesquioxane core." Journal of the Chemical Society, Dalton Transactions, no. 9 (April 3, 2002): 1997–2008. http://dx.doi.org/10.1039/b200303a.

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14

Butler, Ian R., William R. Cullen, Brian E. Mann, and Charles R. Nurse. "Hydrogenation of cationic bis(tertiary alkylphosphine)rhodium(I) complexes. An NMR study." Journal of Organometallic Chemistry 280, no. 2 (January 1985): c47—c50. http://dx.doi.org/10.1016/0022-328x(85)88103-1.

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15

Kharel, Sugam, Kyle J. Cluff, Nattamai Bhuvanesh, John A. Gladysz, and Janet Blümel. "Structures and Dynamics of Secondary and Tertiary Alkylphosphine Oxides Adsorbed on Silica." Chemistry – An Asian Journal 14, no. 15 (July 3, 2019): 2704–11. http://dx.doi.org/10.1002/asia.201900632.

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16

Goodwin, Nicholas J., William Henderson, and Brian K. Nicholson. "An air-stable, primary alkylphosphine: FcCH2PH2 [Fc = (η5-C5H5)Fe(η5-C 5H4)]." Chemical Communications, no. 1 (1997): 31–32. http://dx.doi.org/10.1039/a606580e.

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17

Cavaye, Hamish, Francis Clegg, Peter J. Gould, Melissa K. Ladyman, Tracey Temple, and Eleftheria Dossi. "Primary Alkylphosphine–Borane Polymers: Synthesis, Low Glass Transition Temperature, and a Predictive Capability Thereof." Macromolecules 50, no. 23 (November 30, 2017): 9239–48. http://dx.doi.org/10.1021/acs.macromol.7b02030.

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18

Baya, Miguel, María L. Buil, Miguel A. Esteruelas, and Enrique Oñate. "Dehydrogenation of a Coordinated Alkylphosphine as a Method to Prepare Cyclopentadienyl-α- alkenylphosphine-osmium Complexes." Organometallics 23, no. 6 (March 2004): 1416–23. http://dx.doi.org/10.1021/om034378s.

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19

Barber, Thomas, Stephen P. Argent, and Liam T. Ball. "Expanding Ligand Space: Preparation, Characterization, and Synthetic Applications of Air-Stable, Odorless Di-tert-alkylphosphine Surrogates." ACS Catalysis 10, no. 10 (April 24, 2020): 5454–61. http://dx.doi.org/10.1021/acscatal.0c01414.

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20

Paisner, Sara N., Gino G. Lavoie, and Robert G. Bergman. "Formation of planar-chiral alkylphosphine- and aniline-substituted cyclopentadienyl metal complexes and their reactivity toward electrophiles." Inorganica Chimica Acta 334 (May 2002): 253–75. http://dx.doi.org/10.1016/s0020-1693(02)00742-9.

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21

Koo, Kwangmo, and Gregory L. Hillhouse. "Indoline Synthesis via Coupling of Phenethyl Grignard Reagents with Organoazides Mediated by (Alkylphosphine)nickel(II) Complexes." Organometallics 15, no. 12 (January 1996): 2669–71. http://dx.doi.org/10.1021/om960286+.

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22

Hoisang, Watcharaporn, Taro Uematsu, Takahisa Yamamoto, Tsukasa Torimoto, and Susumu Kuwabata. "Core Nanoparticle Engineering for Narrower and More Intense Band-Edge Emission from AgInS2/GaSx Core/Shell Quantum Dots." Nanomaterials 9, no. 12 (December 11, 2019): 1763. http://dx.doi.org/10.3390/nano9121763.

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Highly luminescent silver indium sulfide (AgInS2) nanoparticles were synthesized by dropwise injection of a sulfur precursor solution into a cationic metal precursor solution. The two-step reaction including the formation of silver sulfide (Ag2S) nanoparticles as an intermediate and their conversion to AgInS2 nanoparticles, occurred during the dropwise injection. The crystal structure of the AgInS2 nanoparticles differed according to the temperature of the metal precursor solution. Specifically, the tetragonal crystal phase was obtained at 140 °C, and the orthorhombic crystal phase was obtained at 180 °C. Furthermore, when the AgInS2 nanoparticles were coated with a gallium sulfide (GaSx) shell, the nanoparticles with both crystal phases emitted a spectrally narrow luminescence, which originated from the band-edge transition of AgInS2. Tetragonal AgInS2 exhibited narrower band-edge emission (full width at half maximum, FWHM = 32.2 nm) and higher photoluminescence (PL) quantum yield (QY) (49.2%) than those of the orthorhombic AgInS2 nanoparticles (FWHM = 37.8 nm, QY = 33.3%). Additional surface passivation by alkylphosphine resulted in higher PL QY (72.3%) with a narrow spectral shape.

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23

Duan, Wu, Jing Chen, Jian Wang, Shu Wang, and Xing Wang. "Development of a test system for high level liquid waste partitioning." Nuclear Technology and Radiation Protection 30, no. 4 (2015): 311–17. http://dx.doi.org/10.2298/ntrp1504311d.

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The partitioning and transmutation strategy has increasingly attracted interest for the safe treatment and disposal of high level liquid waste, in which the partitioning of high level liquid waste is one of the critical technical issues. An improved total partitioning process, including a tri-alkylphosphine oxide process for the removal of actinides, a crown ether strontium extraction process for the removal of strontium, and a calixcrown ether cesium extraction process for the removal of cesium, has been developed to treat Chinese high level liquid waste. A test system containing 72-stage 10-mm-diam annular centrifugal contactors, a remote sampling system, a rotor speed acquisition-monitoring system, a feeding system, and a video camera-surveillance system was successfully developed to carry out the hot test for verifying the improved total partitioning process. The test system has been successfully used in a 160 hour hot test using genuine high level liquid waste. During the hot test, the test system was stable, which demonstrated it was reliable for the hot test of the high level liquid waste partitioning.

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24

Amoroso, Dino, Glenn PA Yap, and Deryn E. Fogg. "The life, death, and ROMP activity of ruthenium complexes containing the basic, chelating diphosphine bis(dicyclohexyl)-1,4-phosphinobutane." Canadian Journal of Chemistry 79, no. 5-6 (May 1, 2001): 958–63. http://dx.doi.org/10.1139/v00-208.

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Reaction of RuCl2(PPh3)3 with bis(dicyclohexyl)-1,4-phosphinobutane (dcypb) under N2 affords access to a formerly elusive family of dcypb complexes based on the RuCl2(PP) core. Under Ar or vacuum atmosphere, decomposition occurs via Ru-promoted dehydrogenation of the dcypb ligand. While the N2-stabilized species [RuCl2(dcypb)]2(N2) (4a) is easily handled under N2 in nonchlorinated solvents, reaction with chlorinated solvents rapidly yields paramagnetic Ru2Cl5(dcypb)2 (5). The N2 ligand within 4a is readily displaced under H2 or CO atmosphere, yielding Ru2Cl4(dcypb)2(H2) (6) or RuCl2(dcypb)(CO)2, the latter as a mixture of ccc-(7) and tcc-(8) isomers. Benzylidene derivative RuCl2(dcypb)(CHPh) (1a), prepared in situ by reaction of 4a with PhCHN2, proves exceptionally active in ring-opening metathesis polymerization (ROMP) of norbornene. The X-ray crystal structure of 5 is reported: triclinic, a = 13.390(2), b = 15.726(2), c = 19.524(2) Å, α = 77.325(2), β = 70.964(2), γ = 73.478(2)°, with space group P[Formula: see text] and Z = 2.Key words: ruthenium, alkylphosphine, dehydrogenation, carbene, metathesis, crystal structure.

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25

Watanabe, Eiichi, Yoshinori Hara, Keisuke Wada, and Takeru Onoda. "A NOVEL RHODIUM-TRI-N-ALKYLPHOSPHINE CATALYST SYSTEM FOR THE HYDROGENATION OF CARBON MONOXIDE, FORMALDEHYDE, AND GLYCOLALDEHYDE." Chemistry Letters 15, no. 3 (March 5, 1986): 285–88. http://dx.doi.org/10.1246/cl.1986.285.

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26

Bedford, Robin B., Catherine S. J. Cazin, Michael B. Hursthouse, Mark E. Light, and V�ronique J. M. Scordia. "Di- and tri-alkylphosphine adducts of S-donor palladacycles as catalysts in the Suzuki coupling of aryl chlorides." Dalton Transactions, no. 22 (2004): 3864. http://dx.doi.org/10.1039/b407922c.

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27

Kim, Seong Ju, Seong-Jik Park, and Byung Hwan Um. "Optimization of Acetic Acid Recovery Using Tri-n-alkylphosphine Oxide from Prepulping Extract of Hemicellulose by Response Surface Methodology." Journal of the Korean Wood Science and Technology 44, no. 4 (July 25, 2016): 477–93. http://dx.doi.org/10.5658/wood.2016.44.4.477.

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28

Häp, Markus, Theo Gilles, Thomas Kruck, and Karl-Friedrich Tebbe. "Dichloro[bis(η5-2,4-cyclopentadien-l-yl)alkylphosphan]zirconium: PR(C5H4)2ZrCl2; R = Me, Et, iPr, tBu / Dichloro[bis(η5-2 ,4 -cyclopentadien-l-yl)alkylphosphine]zirconium: PR(C5H4)2ZrCl2; R = Me, Et, iPr, tBu." Zeitschrift für Naturforschung B 54, no. 4 (April 1, 1999): 482–86. http://dx.doi.org/10.1515/znb-1999-0411.

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A series of new ansa-zirconocene dichloride compounds [PR(C5H4)2ZrCl2; R = Me (5), Et (6), iPr (7), tBu (8)] with phosphorus as bridging atom between the cyclopentadienyl rings have been prepared, isolated, and characterised by 1H, 13C, 31P NMR spectroscopy, mass spectrometry and elemental analysis. The X-ray structure of 5 is reported.

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29

Santure, D. J., and A. P. Sattelberger. "Metal-metal bonded complexes of the early transition metals. 10. Tertiary alkylphosphine adducts of tetrakis(trifluoroacetato)dimolybdenum (Mo2(O2CCF3)4)." Inorganic Chemistry 24, no. 21 (October 1985): 3477–82. http://dx.doi.org/10.1021/ic00215a034.

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30

Liu, Lianlian, Song Guo, Jie Ma, Kejing Xu, Jianzhang Zhao, and Tierui Zhang. "Broadband Visible-Light-Harvestingtrans-Bis(alkylphosphine) Platinum(II)-Alkynyl Complexes with Singlet Energy Transfer between BODIPY and Naphthalene Diimide Ligands." Chemistry - A European Journal 20, no. 44 (September 15, 2014): 14282–95. http://dx.doi.org/10.1002/chem.201403780.

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31

Ota, Yusuke, Shingo Ito, Jun-ichi Kuroda, Yoshikuni Okumura, and Kyoko Nozaki. "Quantification of the Steric Influence of Alkylphosphine–Sulfonate Ligands on Polymerization, Leading to High-Molecular-Weight Copolymers of Ethylene and Polar Monomers." Journal of the American Chemical Society 136, no. 34 (August 13, 2014): 11898–901. http://dx.doi.org/10.1021/ja505558e.

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32

Huang, Jie-Sheng, Guang-Ao Yu, Jin Xie, Nianyong Zhu, and Chi-Ming Che. "One-Pot Synthesis of Metal Primary Phosphine Complexes from OPCl2R or PCl2R. Isolation and Characterization of Primary Alkylphosphine Complexes of a Metalloporphyrin." Inorganic Chemistry 45, no. 15 (July 2006): 5724–26. http://dx.doi.org/10.1021/ic060553w.

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33

Liu, Lianlian, Dandan Huang, Sylvia M. Draper, Xiuyu Yi, Wanhua Wu, and Jianzhang Zhao. "Visible light-harvesting trans bis(alkylphosphine) platinum(ii)-alkynyl complexes showing long-lived triplet excited states as triplet photosensitizers for triplet–triplet annihilation upconversion." Dalton Transactions 42, no. 30 (2013): 10694. http://dx.doi.org/10.1039/c3dt50496d.

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34

Liu, Lianlian, Song Guo, Jie Ma, Kejing Xu, Jianzhang Zhao, and Tierui Zhang. "Inside Cover: Broadband Visible-Light-Harvestingtrans-Bis(alkylphosphine) Platinum(II)-Alkynyl Complexes with Singlet Energy Transfer between BODIPY and Naphthalene Diimide Ligands (Chem. Eur. J. 44/2014)." Chemistry - A European Journal 20, no. 44 (October 20, 2014): 14142. http://dx.doi.org/10.1002/chem.201490183.

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35

Ma, Ziling, and Yuanhua Wang. "Dirhodium(ii)/P(t-Bu)3 catalyzed tandem reaction of α,β-unsaturated aldehydes with arylboronic acids." Organic & Biomolecular Chemistry 16, no. 40 (2018): 7470–76. http://dx.doi.org/10.1039/c8ob01997e.

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36

Benson, Michael T., and Thomas R. Cundari. "ChemInform Abstract: Cyclometalation of Alkylphosphines." ChemInform 30, no. 14 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199914316.

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37

Howard, S. T., J. P. Foreman, and P. G. Edwards. "Electronic Structure of Aryl- and Alkylphosphines." Inorganic Chemistry 35, no. 20 (January 1996): 5805–12. http://dx.doi.org/10.1021/ic951553r.

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38

Fox, Peter C., J. Phillip Bowen, and Norman L. Allinger. "MM3 molecular mechanics study of alkylphosphines." Journal of the American Chemical Society 114, no. 22 (October 1992): 8536–44. http://dx.doi.org/10.1021/ja00048a028.

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39

TROTTA, M., B. FUBINI, M. GALLARATE, and M. R. GASCO. "Calorimetric study on the solubilization of butanol by alkylphosphate and alkylphosphate-lecithin systems." Journal of Pharmacy and Pharmacology 45, no. 11 (November 1993): 993–95. http://dx.doi.org/10.1111/j.2042-7158.1993.tb05644.x.

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40

Szabó, M. J., R. K. Szilágyi, and L. Bencze. "dtmm/cosmic molecular mechanics parameters for alkylphosphines." Journal of Molecular Structure: THEOCHEM 427, no. 1-3 (March 1998): 55–64. http://dx.doi.org/10.1016/s0166-1280(97)00173-5.

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41

Ilia, Gheorghe, Adriana Popa, Smaranda Iliescu, Alina Bora, Gheorghe Dehelean, and Aurelia Pascariu. "Synthesis of Mixed Alkylphosphites and Alkylphosphates." Phosphorus, Sulfur, and Silicon and the Related Elements 178, no. 7 (July 2003): 1513–19. http://dx.doi.org/10.1080/10426500307865.

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42

Grellier, Mary, and Sylviane Sabo-Etienne. "Dehydrogenation processes via C–H activation within alkylphosphines." Chem. Commun. 48, no. 1 (2012): 34–42. http://dx.doi.org/10.1039/c1cc14676a.

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43

FOX, P. C., J. P. BOWEN, and N. L. ALLINGER. "ChemInform Abstract: MM3 Molecular Mechanics Study of Alkylphosphines." ChemInform 24, no. 7 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199307227.

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44

Dittrich, Nadeshda, Bernhard Kutscher, and Renate Ulbrich-Hofmann. "Alkylphosphate Esters as Inhibitors of Phospholipase D." Journal of Enzyme Inhibition 11, no. 1 (January 1996): 67–75. http://dx.doi.org/10.3109/14756369609038223.

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45

Herranz, C. "Alkylphosphinic surfactants with C14-C16 fatty chain." Journal of the American Oil Chemists' Society 64, no. 7 (July 1987): 1038–39. http://dx.doi.org/10.1007/bf02542445.

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46

Zschunke, A., M. Riemer, E. Leissring, and K. Issleib. "NMR-Untersuchungen an 1,2-Bis(alkylphosphino)-benzenen und ihren Anionen." Zeitschrift f�r anorganische und allgemeine Chemie 525, no. 6 (June 1985): 35–40. http://dx.doi.org/10.1002/zaac.19855250606.

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47

Grellier, Mary, and Sylviane Sabo-Etienne. "ChemInform Abstract: Dehydrogenation Processes via C-H Activation Within Alkylphosphines." ChemInform 43, no. 14 (March 8, 2012): no. http://dx.doi.org/10.1002/chin.201214222.

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48

Nifant’ev, Ilya E., Anton S. Lyadov, Alexander N. Tavtorkin, Alexey A. Vinogradov, Alexander A. Kochubeev, and Pavel V. Ivchenko. "Branched alkylphosphinic acids demonstrate explicit anti-wear effect." Mendeleev Communications 29, no. 5 (September 2019): 558–60. http://dx.doi.org/10.1016/j.mencom.2019.09.027.

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49

de Pablo Nisa, L., F. A. Sánchez, M. D. Bermejo, and S. Pereda. "GC-EoS extension to alkylphosphate imidazolium ionic liquids." Fluid Phase Equilibria 479 (January 2019): 25–32. http://dx.doi.org/10.1016/j.fluid.2018.09.022.

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50

Salgado-Escobar, Oscar, Alexis Hernández-Guadarrama, Ivan Romero-Estudillo, and Irma Linzaga-Elizalde. "Direct Synthesis of Phosphonates and α-Amino-phosphonates from 1,3-Benzoxazines." Molecules 24, no. 2 (January 15, 2019): 294. http://dx.doi.org/10.3390/molecules24020294.

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A straightforward and novel method for transformation of readily available 1,3-benzoxazines to secondary phosphonates and α-aminophosphonates using boron trifluoride etherate as catalyst is developed. The formation of phosphonates proceeds through ortho-quinone methide (o-QM) generated in situ, followed by a phospha-Michael addition reaction. On the other hand, the α-aminophosphonates were obtained by iminium ion formation and the subsequence nucleophilic substitution of alkylphosphites. This method can be also used for the preparation of o-hydroxybenzyl ethers through oxa-Michael addition.

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