Gotowe bibliografie tematyczne / Alkylphosphine

Gotowa bibliografia na temat „Alkylphosphine”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 20 lutego 2023

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Artykuły w czasopismach na temat "Alkylphosphine"

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Jia, Huiru, Betül Küçüköz, Yongheng Xing, Poulomi Majumdar, Caishun Zhang, Ahmet Karatay, Gul Yaglioglu, Ayhan Elmali, Jianzhang Zhao i 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, nr 45 (2014): 9720–36. http://dx.doi.org/10.1039/c4tc01675k.

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Li, Xiwen, Hua Li, Yongye Zhao, Xiaoying Tang, Sufang Ma, Bing Gong i Minfeng Li. "Facile synthesis of well-defined hydrophilic polyesters as degradable poly(ethylene glycol)-like biomaterials". Polymer Chemistry 6, nr 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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Zhang, Wen, Gang Ye i Jing Chen. "New insights into the uranium adsorption behavior of mesoporous SBA-15 silicas decorated with alkylphosphine oxide ligands". RSC Advances 6, nr 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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Kendall, Alexander J., Daniel T. Seidenkranz i David R. Tyler. "Improved Synthetic Route to Heteroleptic Alkylphosphine Oxides". Organometallics 36, nr 13 (21.06.2017): 2412–17. http://dx.doi.org/10.1021/acs.organomet.7b00304.

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Fang, Ji-Ping, Klaus-Dieter Wantke i Klaus Lunkenheimer. "Evaluation of the Dynamic Surface Tension of Alkylphosphine Oxides". Journal of Physical Chemistry 99, nr 13 (marzec 1995): 4632–38. http://dx.doi.org/10.1021/j100013a038.

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Mimeau, David, Olivier Delacroix, Benoit Join i Annie-Claude Gaumont. "Easy access to alkylphosphine boranes starting from unactivated alkenes". Comptes Rendus Chimie 7, nr 8-9 (sierpień 2004): 845–54. http://dx.doi.org/10.1016/j.crci.2004.02.016.

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Ferrari, M., L. Liggieri, F. Ravera, C. Amodio i R. Miller. "Adsorption Kinetics of Alkylphosphine Oxides at Water/Hexane Interface". Journal of Colloid and Interface Science 186, nr 1 (luty 1997): 40–45. http://dx.doi.org/10.1006/jcis.1996.4579.

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Liggieri, L., F. Ravera, M. Ferrari, A. Passerone i R. Miller. "Adsorption Kinetics of Alkylphosphine Oxides at Water/Hexane Interface". Journal of Colloid and Interface Science 186, nr 1 (luty 1997): 46–52. http://dx.doi.org/10.1006/jcis.1996.4580.

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Jansen, Achim, i Stephan Pitter. "Synthese hemilabiler P,N-Liganden: x-2-Pyridyl-n-alkylphosphine". Monatshefte fuer Chemie/Chemical Monthly 130, nr 6 (1999): 783. http://dx.doi.org/10.1007/s007060050239.

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

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Rozprawy doktorskie na temat "Alkylphosphine"

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Tronoff, Ashley. "Chloride abstraction from ruthenium alkyl bis-diphosphine dichlorides". Science, 2008. http://hdl.handle.net/2123/2801.

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Doctor of Philisophy (PhD)
Despite their early discovery, relatively few classes of ruthenium dinitrogen complexes are known. This work describes the successful coordination of dinitrogen to the electron-rich alkylphosphine cores [RuCl(dmpe)2]+ and [RuCl(depe)2]+ by chloride abstraction from both the cis and trans dichloro derivatives. One such complex, trans-[RuCl(N2)(dmpe)2](BArF24), possesses the most activated ruthenium νNN reported to date. A variety of chloride abstraction agents were tested on the cis and trans isomers of [RuCl2(P-P)2] (P-P = dmpe, depe) with the choice of abstracting agent, anion and solvent all found to significantly affect the outcome. Reaction with silver triflate and trimethylsilyl triflate was found to give dichlororuthenium(III) products, which could be readily reduced to the ruthenium(II) starting materials with common reducing agents, as well as by alcohols and hydrazine. The use of thallium triflate avoided oxidation and led to the formation of the crystallographically characterised polymeric incorporation product, [{trans-[RuCl2(dmpe)2]•Tl(OTf)}n] from trans-[RuCl2(dmpe)2] and the interesting chloride-bridged ruthenium dimer cis-[{Ru(depe)2}2(μ-Cl)2](OTf)2 from trans-[RuCl2(depe)2]. Anion exchange of the complex [{trans-[RuCl2(dmpe)2]•Tl(OTf)}n] with the non-coordinating anion tetrakis(3,5-bis(trifluoromethyl)phenyl)borate resulted in removal of thallium from the system and coordination of dinitrogen to give trans-[RuCl(N2)(dmpe)2](BArF24). Cis-[{Ru(depe)2}2(μ-Cl)2](OTf)2 was found to readily react with a variety of small ligands and gave products such as cis-[RuCl(CO)(depe)2](OTf), cis-[RuCl(NCMe)(depe)2](OTf), cis-[RuCl(CNtBu)(depe)2](OTf), cis-[RuCl(NH3)(depe)2](OTf), cis-[RuCl(N3)(depe)2], and trans-[RuCl(η2-H2)(depe)2](OTf). A preliminary X-ray single crystal structure analysis was conducted on the complex cis-[RuCl(CNtBu)(depe)2](OTf). The thallium(I) salt Tl(BArF24) was found to be an efficient chloride abstraction agent under mild conditions. Reactions with cis- and trans-[RuCl2(depe)2] and cis-[RuCl2(dmpe)2] furnished dinitrogen complexes of the form cis-[{RuCl(P-P)2}2(μ-N2)](BArF24)2, whilst reaction of trans-[RuCl2(dmpe)2] with Tl(BArF24) led to the stable five-coordinate complex trans-[RuCl(dmpe)2](BArF24). Vapour diffusion techniques applied to a solution of cis-[{RuCl(depe)2}2(μ-N2)](BArF24)2 gave rise to crystals of trans-[RuCl(N2)(depe)2](BArF24), on which preliminary X-ray molecular structure analysis was performed. Reactions of both cis-[{Ru(depe)2}2(μ-Cl)2](OTf)2 and trans-[RuCl2(dmpe)2] with high pressure (140 psi) dinitrogen at 140 150°C in methanol or tetrahydrofuran resulted in solvent carbonyl abstraction to afford trans-[RuCl(CO)(depe)2](OTf) and trans-[RuCl(CO)(dmpe)2](Cl) from the depe and dmpe complexes respectively. The molecular structure of trans-[RuCl(CO)(dmpe)2](Cl) was determined via single crystal X-ray structure analysis.
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Campbell, Ann M. "Insight into the syntheses and the reactions of ethylene complexes of iridium (I) alkylphosphines". 2007. http://proquest.umi.com/pqdweb?did=1240709891&sid=4&Fmt=2&clientId=39334&RQT=309&VName=PQD.

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Streszczenie:
Thesis (M.A.)--State University of New York at Buffalo, 2007.
Title from PDF title page (viewed on June 28, 2007) Available through UMI ProQuest Digital Dissertations. Thesis adviser: Atwood, Jim D. Includes bibliographical references.
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Części książek na temat "Alkylphosphine"

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Kolich, C. H., C. D. Schmulbach, J. Towarnicky i E. P. Schram. "Bis(Alkylphosphine)Trichlorotitanium(III) Complexes". W Inorganic Syntheses, 97–102. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132470.ch29.

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Benson, Michael T., i Thomas R. Cundari. "Cyclometallation of Alkylphosphines". W Intermolecular Interactions, 71–81. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_7.

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Quaegebeur, J. P., B. Perly i C. Chachaty. "Molecular Order and Dynamics in Short Chain Alkylphosphate/Water Mesophases". W Surfactants in Solution, 449–64. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-1831-6_36.

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Pietrusiewicz, K. M., i M. Stankevič. "Alcoholysis of Alkylphosphine Derivatives". W Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00294.

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Gaumont, A. C., i M. Gulea. "Elimination from α-Oxygenated Alkylphosphine Oxides". W Ene-X Compounds (X=S, Se, Te, N, P), 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-033-00785.

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Gaumont, A. C., i M. Gulea. "Elimination from β-Heteroatom-Substituted Alkylphosphine Oxides". W Ene-X Compounds (X=S, Se, Te, N, P), 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-033-00788.

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"Alkylphosphate". W Springer Reference Medizin, 75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_310114.

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Hey-Hawkins, E., i A. A. Karasik. "Bis(alkylphosphino)- and Poly(alkylphosphino)alkanes". W Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00107.

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Pietrusiewicz, K. M., i M. Stankevič. "Alcoholysis of Alkylphosphines". W Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00270.

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"Product Class 4: Alkylphosphines". W Category 5, Compounds with One Saturated Carbon Heteroatom Bond, redaktorzy Mathey i Trost. Stuttgart: Georg Thieme Verlag, 2009. http://dx.doi.org/10.1055/sos-sd-042-00071.

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