Статті в журналах з теми "Stannylenes"
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Cabeza, Javier A., Israel Fernández, Pablo García-Álvarez, Rubén García-Soriano, Carlos J. Laglera-Gándara, and Rubén Toral. "Stannylenes based on pyrrole-phosphane and dipyrromethane-diphosphane scaffolds: syntheses and behavior as precursors to PSnP pincer palladium(ii), palladium(0) and gold(i) complexes." Dalton Transactions 50, no. 44 (2021): 16122–32. http://dx.doi.org/10.1039/d1dt02967c.
Повний текст джерелаPahar, Sanjukta, Vishal Sharma, Srinu Tothadi, and Sakya S. Sen. "Pyridylpyrrolido ligand in Ge(ii) and Sn(ii) chemistry: synthesis, reactivity and catalytic application." Dalton Transactions 50, no. 45 (2021): 16678–84. http://dx.doi.org/10.1039/d1dt03136h.
Повний текст джерелаNeumann, Wilhelm P. "Germylenes and stannylenes." Chemical Reviews 91, no. 3 (May 1991): 311–34. http://dx.doi.org/10.1021/cr00003a002.
Повний текст джерелаAl-Allaf, Talal A. K. "Reactions of the Divalent Tin Compounds R2M, R = N(SiMe3)2 or CH(SiMe3)2 with Complexes of the Platinum Group Metals." Journal of Chemical Research 2003, no. 2 (January 2003): 101–4. http://dx.doi.org/10.3184/030823403103173110.
Повний текст джерелаKristinsdóttir, Lilja, Nicola L. Oldroyd, Rachel Grabiner, Alastair W. Knights, Andreas Heilmann, Andrey V. Protchenko, Haoyu Niu, et al. "Synthetic, structural and reaction chemistry of N-heterocyclic germylene and stannylene compounds featuring N-boryl substituents." Dalton Transactions 48, no. 31 (2019): 11951–60. http://dx.doi.org/10.1039/c9dt02449b.
Повний текст джерелаOchiai, Tatsumi, and Shigeyoshi Inoue. "Synthesis of a cyclopentadienyl(imino)stannylene and its direct conversion into halo(imino)stannylenes." RSC Advances 7, no. 2 (2017): 801–4. http://dx.doi.org/10.1039/c6ra27697k.
Повний текст джерелаHsu, Chen-Yuan, Li-Wei Chan, Gene-Hsiang Lee, Shie-Ming Peng, and Ching-Wen Chiu. "Triphenylene-based tris-N-heterocyclic stannylenes." Dalton Transactions 44, no. 34 (2015): 15095–98. http://dx.doi.org/10.1039/c5dt00694e.
Повний текст джерелаNakata, Norio, Narimi Hosoda, Shintaro Takahashi, and Akihiko Ishii. "Chlorogermylenes and -stannylenes stabilized by diimidosulfinate ligands: synthesis, structures, and reactivity." Dalton Transactions 47, no. 2 (2018): 481–90. http://dx.doi.org/10.1039/c7dt04390b.
Повний текст джерелаDe Proft, Frank, Lies Broeckaert, Jan Turek, Aleš Růžička, and Rudolph Willem. "Reactivity of low-oxidation state tin compounds: an overview of the benefits of combining DFT Theory and experimental NMR spectroscopy." Canadian Journal of Chemistry 92, no. 6 (June 2014): 447–61. http://dx.doi.org/10.1139/cjc-2013-0521.
Повний текст джерелаNEUMANN, W. P. "ChemInform Abstract: Germylenes and Stannylenes." ChemInform 22, no. 50 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199150327.
Повний текст джерелаArp, Henning, Christoph Marschner, Judith Baumgartner, Patrick Zark, and Thomas Müller. "Coordination Chemistry of Disilylated Stannylenes with Group 10 d10 Transition Metals: Silastannene vs Stannylene Complexation." Journal of the American Chemical Society 135, no. 21 (May 16, 2013): 7949–59. http://dx.doi.org/10.1021/ja401548d.
Повний текст джерелаHerberhold, Max, Christian Köhler, Wolfgang Milius, and Bernd Wrackmeyer. "New Spiro-Tin Compounds: Reaction of N,N′-Dialkyl Sulfur Diimides with Cyclic Bis(amino)stannylenes - Unexpected Formation of a N-N Bond." Zeitschrift für Naturforschung B 50, no. 12 (December 1, 1995): 1811–17. http://dx.doi.org/10.1515/znb-1995-1207.
Повний текст джерелаRaut, Ravindra K., Padmini Sahoo, Dipti Chimnapure, and Moumita Majumdar. "Versatile coordinating abilities of acyclic N4 and N2P2 ligand frameworks in conjunction with Sn[N(SiMe3)2]2." Dalton Transactions 48, no. 29 (2019): 10953–61. http://dx.doi.org/10.1039/c9dt00617f.
Повний текст джерелаKuriki, Ryunosuke, Takuya Kuwabara, and Youichi Ishii. "Synthesis and structures of diaryloxystannylenes and -plumbylenes embedded in 1,3-diethers of thiacalix[4]arene." Dalton Transactions 49, no. 35 (2020): 12234–41. http://dx.doi.org/10.1039/d0dt02496a.
Повний текст джерелаRoselló-Merino, Marta, and Stephen M. Mansell. "Synthesis and reactivity of fluorenyl-tethered N-heterocyclic stannylenes." Dalton Transactions 45, no. 14 (2016): 6282–93. http://dx.doi.org/10.1039/c5dt04060d.
Повний текст джерелаKhrustalev, Victor N., Ivan A. Portnyagin, Nikolay N. Zemlyansky, Irina V. Borisova, Mikhail S. Nechaev, Yuri A. Ustynyuk, Mikhail Yu Antipin, and Valery Lunin. "New stable germylenes, stannylenes, and related compounds." Journal of Organometallic Chemistry 690, no. 5 (March 2005): 1172–77. http://dx.doi.org/10.1016/j.jorganchem.2004.11.024.
Повний текст джерелаKarwasara, Surendar, Chandan Kumar Jha, Soumen Sinhababu, and Selvarajan Nagendran. "O,S-Heterocyclic stannylenes: synthesis and reactivity." Dalton Transactions 45, no. 17 (2016): 7200–7204. http://dx.doi.org/10.1039/c6dt01013j.
Повний текст джерелаPAETZOLD, P., D. HAHNFELD, and U. ENGLERT. "ChemInform Abstract: Addition of Stannylenes to Iminoboranes." ChemInform 23, no. 34 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199234247.
Повний текст джерелаPiskunov, Alexander V., Igor A. Aivaz’yan, Vladimir K. Cherkasov, and Gleb A. Abakumov. "New paramagnetic N-heterocyclic stannylenes: An EPR study." Journal of Organometallic Chemistry 691, no. 8 (April 2006): 1531–34. http://dx.doi.org/10.1016/j.jorganchem.2005.11.064.
Повний текст джерелаWrackmeyer, Bernd, and Jürgen Weidinger. "N-Boryl-Substituted Bis(amino)stannylenes and -plumbylenes." Zeitschrift für Naturforschung B 52, no. 8 (August 1, 1997): 947–50. http://dx.doi.org/10.1515/znb-1997-0811.
Повний текст джерелаÁlvarez-Rodríguez, Lucía, Javier A. Cabeza, Pablo García-Álvarez, and Diego Polo. "Organic Amides as Suitable Precursors to Stabilize Stannylenes." Organometallics 32, no. 12 (June 13, 2013): 3557–61. http://dx.doi.org/10.1021/om400476c.
Повний текст джерелаKöpper, Sabine, and Anna Brandenburg. "Novel 1,6-Stannylenes of Glucose, Galactose and Mannose." Liebigs Annalen der Chemie 1992, no. 9 (September 17, 1992): 933–40. http://dx.doi.org/10.1002/jlac.1992199201154.
Повний текст джерелаKrupski, Sergei, Christian Schulte to Brinke, Hannah Koppetz, Alexander Hepp, and F. Ekkehardt Hahn. "Protic N-Heterocyclic Germylenes and Stannylenes: Synthesis and Reactivity." Organometallics 34, no. 11 (February 9, 2015): 2624–31. http://dx.doi.org/10.1021/om5012616.
Повний текст джерелаBenet, Sisco, Christine J. Cardin, David J. Cardin, Steven P. Constantine, Peter Heath, Haroon Rashid, Susana Teixeira, James H. Thorpe, and Alan K. Todd. "Syntheses and Crystal Structures of Heteroleptic Stannylenes and Germylenes." Organometallics 18, no. 3 (February 1999): 389–98. http://dx.doi.org/10.1021/om980836z.
Повний текст джерелаSmith, Laura A., Wei-Bo Wang, Cynthia Burnell-Curty, and Eric J. Roskamp. "Conversion of Esters to Amides with Amino Halo Stannylenes." Synlett 1993, no. 11 (1993): 850–52. http://dx.doi.org/10.1055/s-1993-22630.
Повний текст джерелаSindlinger, Christian P., Frederik S. W. Aicher, and Lars Wesemann. "Cationic Stannylenes: In Situ Generation and NMR Spectroscopic Characterization." Inorganic Chemistry 56, no. 1 (December 15, 2016): 548–60. http://dx.doi.org/10.1021/acs.inorgchem.6b02377.
Повний текст джерелаDay, Benjamin M., Philip W. Dyer, and Martyn P. Coles. "Hydroformylation by Pt–Sn compounds from N-heterocyclic stannylenes." Dalton Transactions 41, no. 25 (2012): 7457. http://dx.doi.org/10.1039/c2dt30988b.
Повний текст джерелаÁlvarez-Rodríguez, Lucía, Javier A. Cabeza, Pablo García-Álvarez, and Diego Polo. "The transition-metal chemistry of amidinatosilylenes, -germylenes and -stannylenes." Coordination Chemistry Reviews 300 (September 2015): 1–28. http://dx.doi.org/10.1016/j.ccr.2015.04.008.
Повний текст джерелаSullivan, Hannah S. I., Andrew J. Straiton, Gabriele Kociok-Köhn, and Andrew L. Johnson. "N-O Ligand Supported Stannylenes: Preparation, Crystal, and Molecular Structures." Inorganics 10, no. 9 (August 31, 2022): 129. http://dx.doi.org/10.3390/inorganics10090129.
Повний текст джерелаPaul, Daniel, Frederik Heins, Sergei Krupski, Alexander Hepp, Constantin G. Daniliuc, Kevin Klahr, Johannes Neugebauer, Frank Glorius, and F. Ekkehardt Hahn. "Synthesis and Reactivity of Intramolecularly NHC-Stabilized Germylenes and Stannylenes." Organometallics 36, no. 5 (February 21, 2017): 1001–8. http://dx.doi.org/10.1021/acs.organomet.6b00925.
Повний текст джерелаBareš, Josef, Zdeňka Padělková, Philippe Meunier, Nadine Pirio, and Aleš Růžička. "Reactivity of di-n-butyl-dicyclopentadienylzirconium towards amido stabilized stannylenes." Journal of Organometallic Chemistry 694, no. 9-10 (April 2009): 1263–65. http://dx.doi.org/10.1016/j.jorganchem.2009.01.041.
Повний текст джерелаHuang, Mengmeng, El’mira Kh Lermontova, Kirill V. Zaitsev, Andrei V. Churakov, Yuri F. Oprunenko, Judith A. K. Howard, Sergey S. Karlov, and Galina S. Zaitseva. "Novel germylenes and stannylenes based on pyridine-containing dialcohol ligands." Journal of Organometallic Chemistry 694, no. 23 (November 2009): 3828–32. http://dx.doi.org/10.1016/j.jorganchem.2009.06.039.
Повний текст джерелаMehring, Michael, Christian Löw, Markus Schürmann, Frank Uhlig, Klaus Jurkschat, and Bernard Mahieu. "Novel Heteroleptic Stannylenes with Intramolecular O,C,O-Donor Stabilization†,‡." Organometallics 19, no. 22 (October 2000): 4613–23. http://dx.doi.org/10.1021/om000452k.
Повний текст джерелаKOEPPER, S., and A. BRANDENBURG. "ChemInform Abstract: Novel 1,6-Stannylenes of Glucose, Galactose and Mannose." ChemInform 24, no. 3 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199303253.
Повний текст джерелаWRACKMEYER, B., and J. WEIDINGER. "ChemInform Abstract: N-Boryl-Substituted Bis(amino)stannylenes and -plumbylenes." ChemInform 28, no. 49 (August 2, 2010): no. http://dx.doi.org/10.1002/chin.199749194.
Повний текст джерелаZabula, Alexander V., and F. Ekkehardt Hahn. "Mono- and Bidentate Benzannulated N-Heterocyclic Germylenes, Stannylenes and Plumbylenes." European Journal of Inorganic Chemistry 2008, no. 33 (November 2008): 5165–79. http://dx.doi.org/10.1002/ejic.200800866.
Повний текст джерелаKrebs, K. M., S. Freitag, J. J. Maudrich, H. Schubert, P. Sirsch, and L. Wesemann. "Coordination chemistry of stannylene-based Lewis pairs – insertion into M–Cl and M–C bonds. From base stabilized stannylenes to bidentate ligands." Dalton Transactions 47, no. 1 (2018): 83–95. http://dx.doi.org/10.1039/c7dt04044j.
Повний текст джерелаBaumgartner, Judith, and Christoph Marschner. "Coordination of non-stabilized germylenes, stannylenes, and plumbylenes to transition metals." Reviews in Inorganic Chemistry 34, no. 2 (June 1, 2014): 119–52. http://dx.doi.org/10.1515/revic-2013-0014.
Повний текст джерелаZhou, Dong, Clemens Reiche, Mrinmoy Nag, John A. Soderquist, and Peter P. Gaspar. "Synthesis of 1-Stannacyclopent-3-enes and Their Pyrolysis to Stannylenes." Organometallics 28, no. 8 (April 27, 2009): 2595–608. http://dx.doi.org/10.1021/om800541f.
Повний текст джерелаNechaev, Mikhail S. "New type of reactions of stannylenes with organic azides: Theoretical study." Journal of Molecular Structure: THEOCHEM 862, no. 1-3 (August 2008): 49–52. http://dx.doi.org/10.1016/j.theochem.2008.04.024.
Повний текст джерелаMengmeng, H., S. S. Karlov, M. V. Zabalov, K. V. Zaitsev, D. A. Lemenovskii, and G. S. Zaitseva. "Structures of germylenes and stannylenes with chelating ligands: a DFT study." Russian Chemical Bulletin 58, no. 8 (August 2009): 1576–80. http://dx.doi.org/10.1007/s11172-009-0216-y.
Повний текст джерелаKrupski, Sergei, Julia V. Dickschat, Alexander Hepp, Tania Pape, and F. Ekkehardt Hahn. "Synthesis and Characterization of Rigid Ditopic N-Heterocyclic Benzobisgermylenes and -stannylenes." Organometallics 31, no. 5 (February 29, 2012): 2078–84. http://dx.doi.org/10.1021/om3000604.
Повний текст джерелаAlvarez-Rodriguez, Lucia, Javier A. Cabeza, Pablo Garcia-Alvarez, and Diego Polo. "ChemInform Abstract: The Transition-Metal Chemistry of Amidinatosilylenes, -Germylenes and -Stannylenes." ChemInform 46, no. 51 (December 2015): no. http://dx.doi.org/10.1002/chin.201551206.
Повний текст джерелаBreher, Frank, and Heinz Rüegger. "Distannenes Turned Inside Out: Bis(stannylenes) with an Unusual Structural Motif." Angewandte Chemie International Edition 44, no. 3 (December 29, 2004): 473–77. http://dx.doi.org/10.1002/anie.200460910.
Повний текст джерелаSMITH, L. A., W. B. WANG, C. BURNELL-CURTY, and E. J. ROSKAMP. "ChemInform Abstract: Conversion of Esters to Amides with Amino Halo Stannylenes." ChemInform 25, no. 36 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199436089.
Повний текст джерелаWrackmeyer, Bernd, Andreas Pedall, and Jürgen Weidinger. "N-Silylaminotin Trichlorides. Synthesis and Characterisation by Multinuclear Magnetic Resonance Spectroscopy." Zeitschrift für Naturforschung B 56, no. 10 (October 1, 2001): 1009–14. http://dx.doi.org/10.1515/znb-2001-1008.
Повний текст джерелаŠvec, Petr, Maksim A. Samsonov, Zdeňka Růžičková, Jiří Brus, and Aleš Růžička. "Oxidative addition of cyanogen bromide to C,N-chelated and Lappert's stannylenes." Dalton Transactions 50, no. 16 (2021): 5519–29. http://dx.doi.org/10.1039/d1dt00704a.
Повний текст джерелаBankiewicz, Barbara, and Piotr Matczak. "Controlling the preferred nitrogen site in 1,2,3-triazine to bind with stannylenes." Polyhedron 225 (October 2022): 116056. http://dx.doi.org/10.1016/j.poly.2022.116056.
Повний текст джерелаDickschat, Julia V., Slawomir Urban, Tania Pape, Frank Glorius, and F. Ekkehardt Hahn. "Sterically demanding and chiral N,N′-disubstituted N-heterocyclic germylenes and stannylenes." Dalton Transactions 39, no. 48 (2010): 11519. http://dx.doi.org/10.1039/c0dt01233e.
Повний текст джерелаŠvec, Petr, Zdeňka Padělková, Mercedes Alonso, Frank De Proft, and Aleš Růžička. "Comparison of reactivity of C,N-chelated and Lappert’s stannylenes with trimethylsilylazide." Canadian Journal of Chemistry 92, no. 6 (June 2014): 434–40. http://dx.doi.org/10.1139/cjc-2013-0500.
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