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1.
Summary Using a saturated non-boiling hydrocarbon mixture, the influence of two parameters on the results of field ionization mass spectrometry (FI-MS) measurements was studied: (a) the potential difference between the FI emitter and the counterelectrode; (b) the emitter temperature.Variation of the potential difference had only a minor effect on the average molecular mass measured and had no evident effect on the relative ring number distribution in the sample. In contrast, when the emitter temperature was increased, higher average molecular masses were recorded. Moreover, the average molecular masses shifted to higher ring numbers. In order to control the relationship between the described influences during mixture analysis, measuring instructions have been developed that enable the quantitative analysis of unknown saturated samples. However, average molecular mass of the mixture must be known.
Entwicklung einer quantitativen FI-MS-Methode zur Charakterisierung von gesättigten hoch- und nichtsiedenden Kohlenwasserstoffgemischen相似文献
2.
Watson MD Jäckel F Severin N Rabe JP Müllen K 《Journal of the American Chemical Society》2004,126(5):1402-1407
Cyclophanes with the largest-to-date polycyclic aromatic hydrocarbon (hexa-peri-hexabenzocoronene, HBC) to be entrained in such a structural motif are reported. The two disks are covalently captured by intermolecular ring-closing olefin metathesis of dienes in good yield. DSC, optical microscopy, and WAXD show the new cyclophanes to self-assemble to thermotropic columnar liquid crystal mesophases similar to monomeric analogues. Solution spectroscopic studies reveal that the two disks within a single unit lie face-to-face, with a small average lateral offset. Self-assembly into two-dimensional crystals at a solid-liquid interface was visualized by STM, and the electrical properties of single molecules were assessed by scanning tunneling spectroscopy revealing a diode-like behavior which is similar to that previously reported for single HBC disks, laying the groundwork for future electrical interrogations of dynamic molecular complexes. 相似文献
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Résumé L'analyse de coupes lourdes (huile de distillation sous vide et huile issue du séparateur à chaud) provenant de l'hydroliquéfaction
catalytique du charbon a été réalisée par mise en ouvre de différentes techniques chromatographiques. L'identification des
principales structures résulte de l'application de la chromatographie par couplage de transfert de charge en mode HPLC et
des spectroscopies UV et de masse.
Donotor-acceptor complex chromatography —Application to analysis of coal liquefaction products by HPLC
Summary A Vacuum gas oil and the corresponding residue of a coal liquefaction product were investigated by means of HPLC and MS. Nearly a complete identification was performed by chromatographic, UV-spectroscopic methods and MS.
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R. M. Khomutov E. S. Severin G. K. Kovaleva N. V. Gnuchev 《Russian Chemical Bulletin》1967,16(8):1743-1745
Conclusions Various O-substituted hydroxylamines were synthesized by the method proposed by us.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1820–1823, August, 1967. 相似文献
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Dr. Zhaowen Dong Dr. Andrzej Sienkiewicz Dr. Abdusalom A. Suleymanov Cesare Berton Dr. Farzaneh Fadaei-Tirani Dr. Rosario Scopelliti Prof. Kay Severin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(32):e202200893
Dichalcogenolenes are archetypal redox non-innocent ligands with numerous applications. Herein, a diselenolene ligand with fundamentally different electronic properties is described. A mesoionic diselenolene was prepared by selenation of a C2-protected imidazolium salt. This ligand is diamagnetic, which is in contrast to the paramagnetic nature of standard dichalcogenolene monoanions. The new ligand is also redox-active, as demonstrated by isolation of a stable diselenolene radical dianion. The unique electronic properties of the new ligand give rise to unusual coordination chemistry. Thus, preparation of a hexacoordinate aluminum tris(diselenolene) complex and a Lewis acidic aluminate complex with two ligand-centered unpaired electrons was achieved. 相似文献