Letteratura scientifica selezionata sul tema "Alkylphosphine"
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Articoli di riviste sul tema "Alkylphosphine"
Jia, Huiru, Betül Küçüköz, Yongheng Xing, Poulomi Majumdar, Caishun Zhang, Ahmet Karatay, Gul Yaglioglu, Ayhan Elmali, Jianzhang Zhao e 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, n. 45 (2014): 9720–36. http://dx.doi.org/10.1039/c4tc01675k.
Testo completoLi, Xiwen, Hua Li, Yongye Zhao, Xiaoying Tang, Sufang Ma, Bing Gong e Minfeng Li. "Facile synthesis of well-defined hydrophilic polyesters as degradable poly(ethylene glycol)-like biomaterials". Polymer Chemistry 6, n. 36 (2015): 6452–56. http://dx.doi.org/10.1039/c5py00762c.
Testo completoZhang, Wen, Gang Ye e Jing Chen. "New insights into the uranium adsorption behavior of mesoporous SBA-15 silicas decorated with alkylphosphine oxide ligands". RSC Advances 6, n. 2 (2016): 1210–17. http://dx.doi.org/10.1039/c5ra21636b.
Testo completoKendall, Alexander J., Daniel T. Seidenkranz e David R. Tyler. "Improved Synthetic Route to Heteroleptic Alkylphosphine Oxides". Organometallics 36, n. 13 (21 giugno 2017): 2412–17. http://dx.doi.org/10.1021/acs.organomet.7b00304.
Testo completoFang, Ji-Ping, Klaus-Dieter Wantke e Klaus Lunkenheimer. "Evaluation of the Dynamic Surface Tension of Alkylphosphine Oxides". Journal of Physical Chemistry 99, n. 13 (marzo 1995): 4632–38. http://dx.doi.org/10.1021/j100013a038.
Testo completoMimeau, David, Olivier Delacroix, Benoit Join e Annie-Claude Gaumont. "Easy access to alkylphosphine boranes starting from unactivated alkenes". Comptes Rendus Chimie 7, n. 8-9 (agosto 2004): 845–54. http://dx.doi.org/10.1016/j.crci.2004.02.016.
Testo completoFerrari, M., L. Liggieri, F. Ravera, C. Amodio e R. Miller. "Adsorption Kinetics of Alkylphosphine Oxides at Water/Hexane Interface". Journal of Colloid and Interface Science 186, n. 1 (febbraio 1997): 40–45. http://dx.doi.org/10.1006/jcis.1996.4579.
Testo completoLiggieri, L., F. Ravera, M. Ferrari, A. Passerone e R. Miller. "Adsorption Kinetics of Alkylphosphine Oxides at Water/Hexane Interface". Journal of Colloid and Interface Science 186, n. 1 (febbraio 1997): 46–52. http://dx.doi.org/10.1006/jcis.1996.4580.
Testo completoJansen, Achim, e Stephan Pitter. "Synthese hemilabiler P,N-Liganden: x-2-Pyridyl-n-alkylphosphine". Monatshefte fuer Chemie/Chemical Monthly 130, n. 6 (1999): 783. http://dx.doi.org/10.1007/s007060050239.
Testo completoKim, Dae-Jin, Ju-Hyun Lee, Jae-Woong Yu, Eui Jung Kim e Kee-Kahb Koo. "Low temperature non-alkylphosphine based synthesis of cadmium selenide nanocrystals". Colloids and Surfaces A: Physicochemical and Engineering Aspects 313-314 (febbraio 2008): 211–15. http://dx.doi.org/10.1016/j.colsurfa.2007.04.096.
Testo completoTesi sul tema "Alkylphosphine"
Tronoff, Ashley. "Chloride abstraction from ruthenium alkyl bis-diphosphine dichlorides". Science, 2008. http://hdl.handle.net/2123/2801.
Testo completoDespite 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.
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.
Testo completoTitle from PDF title page (viewed on June 28, 2007) Available through UMI ProQuest Digital Dissertations. Thesis adviser: Atwood, Jim D. Includes bibliographical references.
Capitoli di libri sul tema "Alkylphosphine"
Kolich, C. H., C. D. Schmulbach, J. Towarnicky e E. P. Schram. "Bis(Alkylphosphine)Trichlorotitanium(III) Complexes". In Inorganic Syntheses, 97–102. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132470.ch29.
Testo completoBenson, Michael T., e Thomas R. Cundari. "Cyclometallation of Alkylphosphines". In Intermolecular Interactions, 71–81. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_7.
Testo completoQuaegebeur, J. P., B. Perly e C. Chachaty. "Molecular Order and Dynamics in Short Chain Alkylphosphate/Water Mesophases". In Surfactants in Solution, 449–64. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-1831-6_36.
Testo completoPietrusiewicz, K. M., e M. Stankevič. "Alcoholysis of Alkylphosphine Derivatives". In Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00294.
Testo completoGaumont, A. C., e M. Gulea. "Elimination from α-Oxygenated Alkylphosphine Oxides". In 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.
Testo completoGaumont, A. C., e M. Gulea. "Elimination from β-Heteroatom-Substituted Alkylphosphine Oxides". In 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.
Testo completo"Alkylphosphate". In Springer Reference Medizin, 75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_310114.
Testo completoHey-Hawkins, E., e A. A. Karasik. "Bis(alkylphosphino)- and Poly(alkylphosphino)alkanes". In Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00107.
Testo completoPietrusiewicz, K. M., e M. Stankevič. "Alcoholysis of Alkylphosphines". In Organophosphorus Compounds (incl. RO-P and RN-P), 1. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-042-00270.
Testo completo"Product Class 4: Alkylphosphines". In Category 5, Compounds with One Saturated Carbon Heteroatom Bond, a cura di Mathey e Trost. Stuttgart: Georg Thieme Verlag, 2009. http://dx.doi.org/10.1055/sos-sd-042-00071.
Testo completo