| 2 | Author
| Christian Müller, ThomasG. Meyer, Michael Farkens, R.Alf Sonnenburg, Reinhard Schmutzler | Requires cookie* | | Title
| Zur Chemie der 4,6-D ioxo-l,3,5,2 A3-triazaphosphinane. Teil II*. Darstellung von 4,6-Dioxo-l,3>5,2 A3-triazaphosphinanen  | | |
Reference
| Z. Naturforsch. 47b, 760—7 (1992); eingegangen am 30. Dezember 1991 | | |
Published
| 1992 | | |
Keywords
| 1, 3, 5-Triorganosubstituted Biurets, 1, 3, 5-Triorgano-Substituted 4, 6-D ioxo-l, 3, 5, 2A 3-triazaphosphinanes, N M R Spectra, M ass Spectra | | |
Similar Items
| Find | | DEBUG INFO
| | | | TEI-XML for
| default:Reihe_B/47/ZNB-1992-47b-0760.pdf | | | Identifier
| ZNB-1992-47b-0760 | | | Volume
| 47 | |
3 | Author
| Wolfram Bodenmüller, Andreas Ruoff, Laurent Manceron | Requires cookie* | | Title
| FTIR Study of the v 12 and the v 12 + v 14 — v 14 Bands of 1,3,5-Triazine Near 740 cm -1  | | | Abstract
| The infrared spectrum of the v 12 fundamental and its accompanying hot band v 12 + v 14 — v 14 of triazine has been measured by means of a Fourier transform spectrometer with a resolution of about 0.0023 cm" 1 . A total of about 2779 rovibrational transitions has been assigned. The ground state constants have been considerably improved whilst the parameters for the excited states tf 12 =l, i; 14 = l and tf 12 =i> 14 = l have been obtained for the first time. The standard deviations were 2.92 • 10" 4 cm" 1 for the ground state constants and 1.53 • 10" 4 cm 1 for the excited state parame-ters of v 12 showing the latter to be unperturbed. The upper state of the hot band v 12 + v 14 — v 14 was found to be perturbed by an accidental resonance. | | |
Reference
| Z. Naturforsch. 47a, 1197—1203 (1992); received October 20 1992 | | |
Published
| 1992 | | |
Keywords
| 1, 3, 5-triazine, High resolution FTIR spectroscopy, Ground state constants Funda-mental constants, Hot band constants | | |
Similar Items
| Find | | DEBUG INFO
| | | | TEI-XML for
| default:Reihe_A/47/ZNA-1992-47a-1197.pdf | | | Identifier
| ZNA-1992-47a-1197 | | | Volume
| 47 | |
4 | Author
| N. Orbert Auner, Erika Penzenstadler | Requires cookie* | | Title
| Silaheterocyclen, XVII Synthese und Cycloadditionsreaktionen neuartiger, aminocyclischer Silaethene [1] Silaheterocycles, XVII Synthesis and Cycloaddition Reactions of Novel Amino Cyclic Silenes [1]  | | | Abstract
| The silene 2 is formed by reacting 2-chloro-l,3-bis(trimethylsilyl)-2-vinyl-1,3-diaza-2-silacyclopentane (5) with LiBu' in «-pentane in the tem perature range from -1 0 to +10 °C. The reaction primarily leads to the corresponding a-lithio adduct 6 by addition of the Li-organyl to the vinyl group o f 5; subsequent 1,2-LiCl elimination yields 2 as an intermediate. 2 can be trapped by polar reagents M e3SiX (X = OMe, 0 S 0 2C F 3) as well as by organic dienes which add across the Si = C bond; in the absence of trapping agents, trisilacyclohexane 7 is isolated. The cycloaddition behaviour of 2 is best described by the two mesomeric formulae (a) and (ß), with competitive [4+2] and [2 + 2] addition routes: While with butadienes and norbor-na-2,5-diene the [2 + 2] products are formed mainly in a multiple step reaction via zwitterionic intermediates (1,4 dipoles), the ratio o f the [4+2]/[2 + 2] derivatives from 2 and cyclohexa-1,3-diene becomes nearly equivalent. 2 is thus quite com parable in its reactivity to dichloro-neopentylsilene, Cl2Si = C H C H 2Bu'. | | |
Reference
| Z. Naturforsch. 47b, 795—804 (1992); eingegangen am 25. November 1991 | | |
Published
| 1992 | | |
Keywords
| Silaheterocycles, Synthesis, 1, 3-Bis(trimethylsilyl)-1, 3-diaza-2-silacyclopentane, F orm ation o f Silenes, Cycloaddition Reactions | | |
Similar Items
| Find | | DEBUG INFO
| | | | TEI-XML for
| default:Reihe_B/47/ZNB-1992-47b-0795.pdf | | | Identifier
| ZNB-1992-47b-0795 | | | Volume
| 47 | |
|