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Journal articles on the topic 'PCl2N'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Heston, Amy J., Matthew J. Panzner, Wiley J. Youngs, and Claire A. Tessier. "Lewis Acid Adducts of [PCl2N]3." Inorganic Chemistry 44, no. 19 (2005): 6518–20. http://dx.doi.org/10.1021/ic050974y.

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2

Heston, Amy J., Matthew Panzner, Wiley J. Youngs, and Claire A. Tessier. "ACID-BASE CHEMISTRY OF [PCl2N]3." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 4-5 (2004): 831–37. http://dx.doi.org/10.1080/10426500490427277.

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3

Tun, Zin-Min, Amy J. Heston, Matthew J. Panzner, et al. "Group 13 Superacid Adducts of [PCl2N]3." Inorganic Chemistry 55, no. 7 (2016): 3283–93. http://dx.doi.org/10.1021/acs.inorgchem.5b02341.

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4

Akbari, Alireza, Hoda Ghatezadeh, Babak Golzadeh, and Sattar Arshadi. "Donor Acceptor Bond in [NPCl2]3—MCl3Adducts, a DFT Study and Comparison of Results with Experimental X-Ray Data." E-Journal of Chemistry 9, no. 4 (2012): 2097–107. http://dx.doi.org/10.1155/2012/516040.

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Molecular structures of [PCl2N]3-MCl3adducts, M=B, Al, Ga, In, Tl, have been studied employing HF, B3LYP*, B3LYP , PW91, BLYP, OLYP, BP and LDA methods using DZP basis set (as defined in Amsterdam Density Functional, ADF, package). Some aspects of adduct formation like considering the difference between Front and Back dihedral angles and also ring puckering showed that the [PCl2N]3-AlCl3is the most stable adduct comparing the others. Based on the comparison between the X-ray and theoretical geometrical parameters of [NPCl2]3(AlCl3) and [NPCl2]3(GaCl3), the LDA method and BP, PW91 and OLYP func

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5

Tun, Zin-Min, Amy J. Heston, Matthew J. Panzner, et al. "Group 13 Lewis Acid Adducts of [PCl2N]3." Inorganic Chemistry 50, no. 18 (2011): 8937–45. http://dx.doi.org/10.1021/ic201075z.

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6

Tessier, Claire A., and et al et al. "ChemInform Abstract: Group 13 Lewis Acid Adducts of [PCl2N]3." ChemInform 42, no. 48 (2011): no. http://dx.doi.org/10.1002/chin.201148008.

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7

Lenburg, Marc E., and Erin K. O’Shea. "Genetic Evidence for a Morphogenetic Function of the Saccharomyces cerevisiae Pho85 Cyclin-Dependent Kinase." Genetics 157, no. 1 (2001): 39–51. http://dx.doi.org/10.1093/genetics/157.1.39.

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Abstract The Saccharomyces cerevisiae PHO85 gene encodes a nonessential cyclin-dependent kinase that associates with 10 cyclin subunits. To survey the functions provided by Pho85, we identified mutants that require PHO85 for viability. We identified mutations that define seven Pho Eighty-Five Requiring or Efr loci, six of which are previously identified genes—BEM2 (YER155C), SPT7 (YBR081C), GCR1 (YPL075W), SRB5 (YGR104C), HFI1 (YPL254W), and BCK1 (YJL095W)—with one novel gene (YMR212C). We found that mutations in the EFR genes involved in morphogenesis are specifically inviable when the Pho85-

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8

Roy, Matthew M. D., Linkun Miao, Michael J. Ferguson, Robert McDonald, and Eric Rivard. "An unexpected Staudinger reaction at an N-heterocyclic carbene-carbon center." Canadian Journal of Chemistry 96, no. 6 (2018): 543–48. http://dx.doi.org/10.1139/cjc-2017-0607.

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The previously unreported carbene-phosphine adduct (IPr)PCl2N3 [IPr = (HCNDipp)2C:; Dipp = 2,6-iPr2C6H3] was synthesized and used as a synthon toward the elusive dichlorophosphazene monomer unit, [Cl2P=N]. (IPr)PCl2N3 was found to undergo halide and azide abstraction when combined with various electrophiles and its thermolysis yielded the unexpected Staudinger reaction product (IPr=N)PCl2.

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9

Heston, Amy J., Debasish Banerjee, Peter L. Rinaldi, and Claire A. Tessier. "NMR Characterization of the Higher Molecular Weight Byproducts Formed During the Synthesis of [PCl2N]3." Journal of Inorganic and Organometallic Polymers and Materials 17, no. 2 (2007): 477–81. http://dx.doi.org/10.1007/s10904-007-9135-2.

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10

Bougeard, Daniel, Claude Bremard, Roger De Jaeger, and Yahia Lemmouchi. "Conformational stability and force field of short-chain linear chlorophosphazenes: MNDO calculations, phosphorus-31 NMR, vibrational spectra, and normal coordinate analyses of Cl3PN(PCl2N)nP(O)Cl2 and [Cl3PN(PCl2N)nPCl3][PCl6] (n = 1, 2)." Journal of Physical Chemistry 96, no. 22 (1992): 8850–55. http://dx.doi.org/10.1021/j100201a031.

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11

Thome, Benjamin S., Savannah R. Snyder, Joanna M. Beres, et al. "Chlorine/oxygen transfer reactions of [PCl2N]3 using oxygenated Lewis bases as a possible route to [PON]3." Phosphorus, Sulfur, and Silicon and the Related Elements 191, no. 4 (2016): 671–74. http://dx.doi.org/10.1080/10426507.2015.1128934.

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12

Rivard, Eric, Alan J. Lough, and Ian Manners. "A New, Convenient Synthesis of the Linear Phosphazene Salt [Cl3PNPCl3]Cl: Preparation of Higher Linear Homologues [Cl3PN−(PCl2N)xPCl3]Cl (x= 1−3) and the 16-Membered Macrocycle [NCCl(NPCl2)3]2." Inorganic Chemistry 43, no. 9 (2004): 2765–67. http://dx.doi.org/10.1021/ic049955z.

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13

Latifzadeh, Lida, and K. Balasubramanian. "Electronic states of PCl2 and PCl2+." Chemical Physics Letters 241, no. 1-2 (1995): 13–20. http://dx.doi.org/10.1016/0009-2614(95)00551-e.

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14

Hager, Rudolf, and Johann Weis. "Phosphazen-Katalyse. Grundlage der Lineartechnologie zur Siliconherstellung / Phosphazene Catalysis. The Basis of L inear Technology for Silicone Production." Zeitschrift für Naturforschung B 49, no. 12 (1994): 1774–80. http://dx.doi.org/10.1515/znb-1994-1223.

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The structure of the chlorophosphazenes used as catalyst for the polycondensation of siloxanoles to various high molecular weight silicone polymers in the industrial scale has been determined as [PCl3=N(-PCl2=N)x-PCl3]+[PCl6]-. mainly with x=1 and x=2. For better un derstanding of the catalytic mechanism, the reaction behaviour of these ionic phosphazenes with water and siloxanes has been studied. Thereby three further types of phosphazenes have been synthesized: PCl3=N(-PCl2=N)x-PCl2=O,HO-PCl2=N(-PCl2=N)x-PCl2=O and siloxy derivatives of the latter ≡Si-O-PCl2=N(-PCl2=N)x-PCl2=O. Although sev

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15

Eckert, Christine, Lutz Dahlenburg, and Alexander Wolski. "Oligophosphan-Liganden, XXXIX. (1S,2S)-trans-Cyclopentan-1,2-diyl-bis(phosphan), C5H8(PH2)2, durch Reduktion eines diastereomerenreinen Cyclopentandiyl-bis(dioxaphospholans) / Oligophosphine Ligands, XXXIX. (1 S,2S)-trans-Cyclopentane-1,2-diyl-bis(phosphine), C5H8(PH2)2, by Reduction of a Diastereomerically Pure Cyclopentanediyl-bis(dioxaphospholane)." Zeitschrift für Naturforschung B 50, no. 7 (1995): 1004–8. http://dx.doi.org/10.1515/znb-1995-0703.

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The title compound (S,S)-2, has been obtained by reduction with Li[AlH4] of the cyclopentane- 1,2-diyl-bis(1′,3′,2′-dioxaphospholane) (1S ,2S)-trans-C5H8[P(OCH (CO2Pr-i)- (R) - )2]2, (S,S)-1, which itself was isolated in diastereomerically pure form (X-ray structure analysis) from the reaction between rac, trans-C5H8(PCl2)2 and (2R,3R)-(+)-diisopropyl tartrate. Cleavage of (S,.S)-1 withPCl3 yielded an unseparable mixture of (1S,2S)-trans-C5H8(PCl2)2 and (4R.5R) -ClP [OCH(CO2Pr-i)-]2.

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16

Aerne, Birgit L., Anthony L. Johnson, Jeremy H. Toyn, and Leland H. Johnston. "Swi5 Controls a Novel Wave of Cyclin Synthesis in Late Mitosis." Molecular Biology of the Cell 9, no. 4 (1998): 945–56. http://dx.doi.org/10.1091/mbc.9.4.945.

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We have shown previously that the Swi5 transcription factor regulates the expression of the SIC1 Cdk inhibitor in late mitosis. This suggests that Swi5 might control other genes with roles in ending mitosis. We identified a gene with a Swi5-binding site in the promoter that encoded a protein with high homology to Pcl2, a cyclin-like protein that associates with the Cdk Pho85. This gene,PCL9, is indeed regulated by Swi5 in late M phase, the only cyclin known to be expressed at this point in the cell cycle. The Pcl9 protein is associated with a Pho85-dependent protein kinase activity, and the pr

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17

Meyer, Thomas G., Peter G. Jones, and Reinhard Schmutzler. "Darstellung neuer Monofluorphosphine und einiger ihrer Übergangsmetallkomplexe; Einkristall-Röntgenstrukturanalyse eines Platin(II)-Komplexes / Preparation of New Monofluorophosphines and Some of their Transition Metal Complexes; Single Crystal X-Ray Diffraction Study of a Platinum(II) Complex." Zeitschrift für Naturforschung B 48, no. 7 (1993): 875–85. http://dx.doi.org/10.1515/znb-1993-0704.

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The reaction of lithiated precursors with PCl2F led to a number of monofluorophosphines, including the known di-tert-butylmonofluorophosphine, 1. Bis(phenylethinyl)monofluorophosphine (2) was accessible only via this route (the classical method of synthesizing 2 by chlorine/fluorine exchange is impossible, because the corresponding chlorophosphine is unknown). Bis(2-methoxyphenyl)fluorophosphine (5) was prepared via the organolithium/PCl2F route. The NMR results for 5 thus prepared were inconsistent with previous reports, implying that the previously reported synthesis of 5 is in error. From 5

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18

Allen, Christine, Yisong Yu, Adi Eisenberg, and Dusica Maysinger. "Cellular internalization of PCL20-b-PEO44 block copolymer micelles." Biochimica et Biophysica Acta (BBA) - Biomembranes 1421, no. 1 (1999): 32–38. http://dx.doi.org/10.1016/s0005-2736(99)00108-x.

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19

Li, Haichang. "PCL2, a novel tumor suppressor in breast cancer." Science Bulletin 63, no. 10 (2018): 597–98. http://dx.doi.org/10.1016/j.scib.2018.04.004.

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20

Wiberg, Nils, Angelika Wörner, Hans-Wolfram Lerner, and Konstantin Karaghiosoff. "Zur Reaktion von PCl3 mit NaR*, KR* und ZnR*2 (R* = SitBu3) [1]: Bildung des Diphosphens R*P=PR*, Tetraphosphans P4R*2 , Tetraphosphanids NaP4R*3 sowie von Halogenphosphanen R*mPmClp / On the Reaction of PCl3 with NaR*, KR* and ZnR*2 (R*= SitBu3) [1]: Formation of the Diphosphene R*P=PR*, Tetraphosphane P4R*2, Tetraphosphanide NaP4R*3 as well as Halogenophosphanes R*mPnClp." Zeitschrift für Naturforschung B 57, no. 9 (2002): 1027–35. http://dx.doi.org/10.1515/znb-2002-0909.

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The reaction of PCl3 at r. t. with an equimolar amount of NaR* in heptane gives the colorless phosphane R*PCl2 (1), the colorless diphosphane R*ClP-PClR* (2), the light green diphosphene R*P=PR* (4), the cyclotetraphosphane R*2P4Cl2 (6) (not isolated), the light yellow bis(cyclotriphosphanyl) P6R*4 (7), the cyclotriphosphane R*2P3Cl (8) (not isolated), and the colorless bicyclophosphane P4R*2 (9).With a threefold molar amount of NaR* in tetrahydrofuran the blue violet triphosphanide NaP3R*2 (10), the dark red tetraphosphanide NaP4R*3 (11), and the orange pentaphosphanediide Na2P5R*3 (12) are f

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21

Friesen, Helena, Kelly Murphy, Ashton Breitkreutz, Mike Tyers, and Brenda Andrews. "Regulation of the Yeast Amphiphysin Homologue Rvs167p by Phosphorylation." Molecular Biology of the Cell 14, no. 7 (2003): 3027–40. http://dx.doi.org/10.1091/mbc.e02-09-0613.

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The yeast amphiphysin homologue Rvs167p plays a role in regulation of the actin cytoskeleton, endocytosis, and sporulation. Rvs167p is a phosphoprotein in vegetatively growing cells and shows increased phosphorylation upon treatment with mating pheromone. Previous work has shown that Rvs167p can be phosphorylated in vitro by the cyclin-dependent kinase Pho85p complexed with its cyclin Pcl2p. Using chymotryptic phosphopeptide mapping, we have identified the sites on which Rvs167p is phosphorylated in vitro by Pcl2p-Pho85p. We have shown that these same sites are phosphorylated in vivo during ve

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22

Marath, Usha. "Issues and Challenges in Psychiatric Consultation-Liaison nurse (PCLn)." International Journal of Psychiatric Nursing 4, no. 2 (2018): 89. http://dx.doi.org/10.5958/2395-180x.2018.00023.3.

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23

Manias-Rothberg, Janet, Harinad Maganti, Christopher Porter, et al. "Polycomb-like 2 (PCL2) is required for hematopoietic development." Experimental Hematology 42, no. 8 (2014): S47. http://dx.doi.org/10.1016/j.exphem.2014.07.175.

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24

Measday, V., L. Moore, R. Retnakaran, et al. "A family of cyclin-like proteins that interact with the Pho85 cyclin-dependent kinase." Molecular and Cellular Biology 17, no. 3 (1997): 1212–23. http://dx.doi.org/10.1128/mcb.17.3.1212.

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In budding yeast, entry into the mitotic cell cycle, or Start, requires the Cdc28 cyclin-dependent kinase (Cdk) and one of its three associated G1 cyclins, Cln1, Cln2, or Cln3. In addition, two other G1 cyclins, Pcl1 and Pcl2, associate with a second Cdk, Pho85, to contribute to Start. Although Pho85 is not essential for viability, Pcl1,2-Pho85 kinase complexes become essential for Start in the absence of Cln1,2-Cdc28 kinases. In addition, Pho85 interacts with a third cyclin, Pho80, to regulate acid phosphatase gene expression. Other cellular roles for Pho85 cyclin-Cdk complexes are suggested

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25

Breitsameter, F., A. Schmidpeter, H. Nöth, and J. Knizek. "Reduktion eines Bis(chlorphenylphosphanyl)methylids zum entsprechenden Diphosphan und Tetraphosphinan Reduction of a Bis(chlorophenylphosphanyl)methylide to the Corresponding Diphosphane and Tetraphosphinane." Zeitschrift für Naturforschung B 54, no. 1 (1999): 1–7. http://dx.doi.org/10.1515/znb-1999-0103.

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The bis(phosphanyl)ylides Ph3PC(PPh2)2, Ph3PC(PPhCl)2 (3) and Ph3PC(PCl2)2 have analogous molecular structures. Details reflect the different charge transfer from the ylide center to the phosphanyl substituents. Chlorination destroys the chirality of 3. Reduction leads to the diphosphane 8 and the 1,2,4,5-tetraphosphinane 9 which are also included in the structural comparison.

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26

Zou, Jian, Helena Friesen, Jennifer Larson, et al. "Regulation of Cell Polarity through Phosphorylation of Bni4 by Pho85 G1 Cyclin-dependent Kinases in Saccharomyces cerevisiae." Molecular Biology of the Cell 20, no. 14 (2009): 3239–50. http://dx.doi.org/10.1091/mbc.e08-12-1255.

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In the budding yeast Saccharomyces cerevisiae, the G1-specific cyclin-dependent kinases (Cdks) Cln1,2-Cdc28 and Pcl1,2-Pho85 are essential for ensuring that DNA replication and cell division are properly linked to cell polarity and bud morphogenesis. However, the redundancy of Cdks and cyclins means that identification of relevant Cdk substrates remains a significant challenge. We used array-based genetic screens (synthetic genetic array or SGA analysis) to dissect redundant pathways associated with G1 cyclins and identified Bni4 as a substrate of the Pcl1- and Pcl2-Pho85 kinases. BNI4 encodes

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27

Riesel, L., and R. Friebe. "Substitutions- und Oxydationsreaktionen des N-Dichlorphosphanyl-triphenylphosphazens, Ph3P?N?PCl2." Zeitschrift f�r anorganische und allgemeine Chemie 604, no. 1 (1991): 85–91. http://dx.doi.org/10.1002/zaac.19916040112.

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28

M'Sadak, M., J. Roncali, and F. Garnier. "Lanthanides — Phthalocyanines complexes : from a diphthalocyanine Pc2Ln to a super complex Pc3Ln2." Journal de Chimie Physique 83 (1986): 211–16. http://dx.doi.org/10.1051/jcp/1986830211.

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29

Kuhn, Norbert, Michael Schultena, Roland Boese, Dieter Bläser, Waldemar A. Brett, and Peter Stellberg. "Synthese, Struktur und Metallierung von 1,3,5-Tris(dimethylamino)benzol / Synthesis, Structure, and Metalation of 1,3,5-Tris(dimethylamino)benzene." Zeitschrift für Naturforschung B 47, no. 9 (1992): 1233–40. http://dx.doi.org/10.1515/znb-1992-0904.

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The synthesis of 1,3,5-tris(dimethylamino)benzene (5, Ar–H) is reported. The X-ray structure of 5 reveals two independent molecules in the unit cell both containing planar arene rings; the puckering of the amino substituents is demonstrated to be a consequence of steric interactions. 5 is metalated by n-butyl-lithium to give the isolable aryl-lithium compound Ar–Li (6) from which the phosphane Ar–PCl2 (7) and silane Ar–SiCl3 (8) are obtained.

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30

Bitterer, Frank, Klaus Peter Langhans, and Othmar Stelzer. "Lineare Oligophosphaalkane, XXVIII [1] Redox-Cyclisierung funktioneller Methylenbisphosphane XRP-CH2-PRX (X = H, C) mit Cyclopolyphosphanen / Linear Oligophosphaalkanes, XXVIII [1] Redox Cyclization of Functional Methylenebisphosphanes XRP-CH2-PRX (X = H, Cl) with Cyclopolyphosphanes." Zeitschrift für Naturforschung B 50, no. 10 (1995): 1521–26. http://dx.doi.org/10.1515/znb-1995-1015.

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Reaction of P-H or P-Cl functional methylenebisphosphanes X (R )P - CH2-P(R)X (X = H, Cl; R = Ph, tBu) with cyclopolyphosphanes (R′P)„ (R′ = Ph, tBu, Me; n = 4, 5) affords cyclocarbatetraphosphanes CH2(RP)2(R′P)2 (2-6 ). The cyclopolyphosphanes (R′P)„ em ployed may be synthesized in situ by reaction of chlorophosphanes R′PCl2 with primary phosphanes R′PH2, LiH or magnesium, respectively, providing a single stage synthesis for unsymmetrically substituted cyclocarbatetraphosphanes.

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31

Thompson, Noreen C. "Reflections on a PCLN Career and the Need for Self-Care." Perspectives In Psychiatric Care 43, no. 2 (2007): 105–7. http://dx.doi.org/10.1111/j.1744-6163.2007.00110.x.

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32

Miller, Thomas M., A. A. Viggiano, Robert A. Morris, and Amy E. Stevens Miller. "GAUSSIAN-2 calculations of the electron affinities of PCln and POCln." Journal of Chemical Physics 111, no. 7 (1999): 3309–10. http://dx.doi.org/10.1063/1.479657.

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33

Fernández, Daniel, Montserrat Guerra, Judit G. Lisoni та ін. "Fibrous Materials Made of Poly(ε-caprolactone)/Poly(ethylene oxide)-b-Poly(ε-caprolactone) Blends Support Neural Stem Cells Differentiation". Polymers 11, № 10 (2019): 1621. http://dx.doi.org/10.3390/polym11101621.

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In this work, we design and produce micron-sized fiber mats by blending poly(ε-caprolactone) (PCL) with small amounts of block copolymers poly(ethylene oxide)m-block-poly(ε-caprolactone)n (PEOm-b-PCLn) using electrospinning. Three different PEOm-b-PCLn block copolymers, with different molecular weights of PEO and PCL, were synthesized by ring opening polymerization of ε-caprolactone using PEO as initiator and stannous octoate as catalyst. The polymer blends were prepared by homogenous solvent mixing using dichloromethane for further electrospinning procedures. After electrospinning, it was fou

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34

Chou, Jung-Chuan, and Chang-Chi Lee. "REALIZATION OF PLATFORM FOR ION CONCENTRATION MEASUREMENT." Biomedical Engineering: Applications, Basis and Communications 21, no. 06 (2009): 385–88. http://dx.doi.org/10.4015/s1016237209001507.

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LabVIEW has complete development and compiler environment, so the display, saved and transmission interface, etc. are compiled by LabVIEW software in this study. LabVIEW and microcontroller can be integrated for the platform of ion concentration measurement, as well as the acquisition of sensing signal can be obtained via microcontroller. Moreover, the pCl and pH value can be separated in platform of ion concentration measurement. Besides, the platform of ion concentration measurement is measured in pCl2 standard solution, the results are between pCl1.83 and pCl2.08. Hence, the platform of ion

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35

Zhao, Jun, Shu Ping Gong, G. Xiong, and X. H. Yu. "Research on Sintering Dynamics and Microwave Dielectric Properties of Bi and Mn Doped Lead-Based Ceramics." Key Engineering Materials 336-338 (April 2007): 316–19. http://dx.doi.org/10.4028/www.scientific.net/kem.336-338.316.

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The sintering dynamics, microstructures and microwave dielectric properties of Bi2O3 and MnO2 co-doped [(Pb,Ca) La](Fe,Nb)O3 (PCLFN) ceramics were investigated. Bi2O3 and MnO2 dopants effectively enhanced bulk densities and reduced sintering temperatures by about 100~140°C. Sintering procedure had significant effect on grain size and porosities of ceramics. Investigation of microstructures revealed that the grain growth was controlled by either volume diffusion or second-order interface mechanism in present ceramics. The potential microwave dielectric properties of εr=91.1,Qf=4870GHz and τf=18

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36

Brum, Jeffrey L., and Jeffrey W. Hudgens. "Multiphoton Ionization Spectroscopy of PCl2 Radicals: Observation of Two New Rydberg States." Journal of Physical Chemistry 98, no. 22 (1994): 5587–90. http://dx.doi.org/10.1021/j100073a001.

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37

Suzuki, Hiroko, Nobuo Nakanishi, and Shozo Yamada. "Nerve growth factor transiently increases tetrahydrobiopterin and total biopterin contents of pheochromocytoma PCl2h cells." Biochemical and Biophysical Research Communications 153, no. 1 (1988): 382–87. http://dx.doi.org/10.1016/s0006-291x(88)81235-x.

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38

Fujita, Shioeki, Yukiko Kunugi, Tomoyo Takayama, and Takashi Taniguchi. "Alteration of Na, K-pump activity in dibutylyl cAMP-induced differentiation of PCl2h cells." Japanese Journal of Pharmacology 58 (1992): 329. http://dx.doi.org/10.1016/s0021-5198(19)49482-1.

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39

Prishchenko, Andrey A., Mikhail V. Livantsov, Olga P. Novikova, Ludmila I. Livantsova, and Valery S. Petrosyan. "Synthesis of bis- and tris-organophosphorus substituted amines and amino acids with PCH2N Fragments." Heteroatom Chemistry 21, no. 6 (2010): 430–40. http://dx.doi.org/10.1002/hc.20616.

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40

Weber, Lothar, Uwe Sonnenberg, H. G. Stammler та Beate Neumann. "Synthese und Struktur von η1-2,4-Diaza-3-phosphapenta-1,4-dien-3-yl-Komplexen des Eisens und Rutheniums / Synthesis and Structure of η1-2,4-Diaza-3-phosphapenta-1,4-dien-3-yl Complexes of Iron and Ruthenium". Zeitschrift für Naturforschung B 46, № 6 (1991): 714–18. http://dx.doi.org/10.1515/znb-1991-0604.

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The dichlorophosphido complexes (η5-C5Me5)(CO)2M–PCl2 (2a: M = Fe; 2 c: M = Ru) react with two equivalents of Ph2C=NSiMe3 to yield the first η1-2,4-diaza-3-phosphapenta-1,4-dien-3-yl complexes (4a,c). Intermediates (η5-C5Me5)(CO)2M–P(Cl)(N=CPh2) (3a,c) are detected by 31P{1H} NMR spectroscopy, the preparation of pure 3a, however, failed. The products 4a, c have been characterized by elemental analysis as well as spectroscopic data (IR, 1H, 13C, 31P NMR, MS). The molecular structure of 4a has been elucidated by single X-ray analysis.

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Saare, Andrea, and Lutz Dahlenburg. "Oligophosphan-Liganden, XL. trans-Cyclopentan-1,2-diyl-bis(dicyclohexylphosphan) und trans-Norbornan-2,3-diyl-bis(dicyclohexylphosphan): Synthese und Enantiomerentrennung. Reaktionen von [trans-C5H8(PCy2 )2 ]PtH(CH2CMe3 ) mit C– H-Bindungen unter achiralen und chiralen Bedingungen / Oligophosphine Ligands, XL. trans-Cyclopentane-1 ,2-diyl-bis(dicyclohexylphosphine) and trans-Norbornane-2,3-diyl-bis(dicyclohexylphosphine): Synthesis and Separation of Enantiomers. Reactions of [trans-C5H8(PCy2)2]PtH (CH2CMe3) with C - H Bonds under Achiral and Chiral Conditions." Zeitschrift für Naturforschung B 50, no. 7 (1995): 1009–17. http://dx.doi.org/10.1515/znb-1995-0704.

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The bis(dicyclohexylphosphines) trans-C5H8(PCy2)2 (1) and trans-C7H10(PCy2)2 (11) (C5H8 = cyclopentane-1,2-diyl, C7 H10 = norbornane-2,3-diyl) were prepared by treatment of the bis(dichlorophosphines) trans-C5H8(PCl2)2 and trans -C7H10(PCl2)2 with CyMgBr. Oxidation with H2O2 in acetone gave the corresponding P,P′-dioxides, trans- C5H8[P(O)C y2]2 (2) and trans-C7H10[P(O)Cy2]2 (12) respectively. Effective optical resolution of 2 was achieved using (2S,3S )-(+)-di-O-benzoyl tartaric acid as a resolving agent. Heating (+)-2 and (-)-2 in neat Ph2SiH2 gave enantiopure 1. Reactions of 1 and 11 with (

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42

Hirano, T. "Null Mutation of PCLN-1/Claudin-16 Results in Bovine Chronic Interstitial Nephritis." Genome Research 10, no. 5 (2000): 659–63. http://dx.doi.org/10.1101/gr.10.5.659.

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Liang, Yiran, Yang Yang, Renbo Guo, et al. "PCL2 regulates p53 stability and functions as a tumor suppressor in breast cancer." Science Bulletin 63, no. 10 (2018): 629–39. http://dx.doi.org/10.1016/j.scib.2018.03.012.

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44

Strand, Andrew, Bonnie Cole, Sarah Leary, and James Olson. "PCLN-04. BRAIN TUMOR PATIENT DERIVED ORTHOTOPIC XENOGRAFTS INDUCE TUMORS OF MOUSE ORIGIN." Neuro-Oncology 20, suppl_2 (2018): i155. http://dx.doi.org/10.1093/neuonc/noy059.573.

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RIESEL, L., and R. FRIEBE. "ChemInform Abstract: Replacement and Oxidation Reactions of N-Dichlorophosphanyl- triphenylphosphazene, Ph3P=N-PCl2." ChemInform 23, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199205214.

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Wang, Kedong, Yiwen Wang, Xue Li, Yufang Liu, and Jinfeng Sun. "Elastic and inelastic low-energy electron collisions with PH2, PF2 and PCl2 radicals." Journal of Physics B: Atomic, Molecular and Optical Physics 53, no. 6 (2020): 065201. http://dx.doi.org/10.1088/1361-6455/ab63aa.

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47

Takara, Satoshi, Andrei S. Batsanov, Douglas J. Schaffer, Michael Takase, Janice A. Kunishige, and Susan J. Lee. "Solid-State Structures oftrans-[RuCl2{Cl2PN(Me)N(Me)PCl2}2] andcis-[MCl2{Cl2PN(Me)N(Me)PCl2}] (M = PtIIand PdII) Studied by X-ray Crystallography and13C CPMAS NMR Spectroscopy." Bulletin of the Chemical Society of Japan 80, no. 9 (2007): 1776–79. http://dx.doi.org/10.1246/bcsj.80.1776.

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48

Weber, Lothar, Iris Schumann, Hans-Georg Stammler та Beate Neumann. "Übergangsmetall-substituierte Diphosphene, XXVI Zum Einfluß des Ringliganden auf Bildungstendenz und Stabilität von Diphosphenyleisenkomplexen des Typs (η5-C5R5)(CO)2Fe-P= P-Mes (Mes = 2,4,6-tBu3C6H2). Röntgenstrukturanalyse von (η5-C5Me4Et)(CO)2Fe-P(SiMe3)2 / Transition Metal Substituted Diphosphenes, XXVI Investigations on the Influence of the Ring Ligand upon Formation and Stability of Diphosphenyl Complexes (η5-C5R5)(CO)2Fe-P=P-Mes (Mes = 2,4,6-tBu3C6H2). X-Ray Analysis of (η5-C5Me4Et)(CO)2Fe-P(SiMe3)2". Zeitschrift für Naturforschung B 47, № 8 (1992): 1134–40. http://dx.doi.org/10.1515/znb-1992-0814.

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The disilylphosphido iron complexes (η5-C5R5)(CO)2Fe-P(SiMe3)2 (1b–d) result from the reaction of the corresponding bromo compounds (η5-C5R5)(CO)2FeBr with LiP(SiMe3)2 · 2 THF. The complexes 2b–d are cleanly converted into the diphosphenyl complexes (η5-C5R5)(CO)2Fe-P=P-Mes* (2b–d) by treatment with equimolar amounts of Mes*PCl2. The products 1b–d and 2b–d have been characterized by elemental analysis as well as spectroscopic data (IR, 1H, 13C, 31P NMR, MS). The molecular structure of η5-C5Me4Et)(CO)2Fe-P(SiMe3)2 (1b) has been established by single-crystal X-ray analysis.

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Meyer, Thomas G., Axel Fischer, Peter G. Jones, and Reinhard Schmutzler. "Darstellung und Einkristall-Röntgenstrukturanalyse einiger Fluorphosphite und Phosphitester / Preparation and Single Crystal X-Ray Diffraction Study of Some Fluorophosphites and Phosphite Esters." Zeitschrift für Naturforschung B 48, no. 5 (1993): 659–71. http://dx.doi.org/10.1515/znb-1993-0516.

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The synthesis of some monofluorophosphite esters from the appropriate hydroxy compound and PCl2F in the presence of a tertiary amine is described. The reaction of 2,2′-dihydroxy-biphenyl with PCl3 in the presence of triethylamine did not furnish the expected chlorophosphite 9; instead, the bridged bisphosphite ester, 10, was obtained. Reaction of the fluorophosphite ester 8 with 3,5-di-tert-butyl-benzoquinone furnished the spiromonofluorophosphorane 12 in which λ5P is part of a five-membered and a seven-membered ring system. Single crystal X-ray diffraction studies were conducted on compounds

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Prishchenko, Andrey A., Mikhail V. Livantsov, Olga P. Novikova, Ludmila I. Livantsova, and Valery S. Petrosyan. "Synthesis of new organophosphorus-substituted mono- and bis(trimethylsilyl)amines with PCH2N fragments and their derivatives." Heteroatom Chemistry 21, no. 2 (2010): 71–77. http://dx.doi.org/10.1002/hc.20580.

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