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Journal articles on the topic 'Systeme chemistry'

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Published: 25 May 2024

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1

Scheffer, F. E. C., and J. Smittenberg. "Über Binäre Systeme. IV. Äthan-Systeme (Fortsetzung)." Recueil des Travaux Chimiques des Pays-Bas 52, no. 11 (September 3, 2010): 982–86. http://dx.doi.org/10.1002/recl.19330521112.

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2

Gutmann, Viktor, and Gerhard Resch. "Molekulare Systeme." Zeitschrift für Chemie 19, no. 11 (August 31, 2010): 406–12. http://dx.doi.org/10.1002/zfch.19790191103.

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3

Gr�ndler, Wolfgang. "Polycyclische benzenoide Systeme." Monatshefte f�r Chemie Chemical Monthly 119, no. 10 (October 1988): 1125–41. http://dx.doi.org/10.1007/bf00809265.

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4

Scheffer, F. E. C., and J. Smittenberg. "Über Binäre Systeme. III. Einige Systeme mit Äthan als flüchtigerer Komponente." Recueil des Travaux Chimiques des Pays-Bas 52, no. 7 (September 3, 2010): 607–14. http://dx.doi.org/10.1002/recl.19330520710.

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5

Ewers, C. "Modulare Systeme." Chemie Ingenieur Technik 81, no. 8 (August 2009): 1236. http://dx.doi.org/10.1002/cite.200990080.

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6

Mayer, Roland, Horst Hartmann, Jürgen Fabian, and Achim Mehlhorn. "Schwefelhaltige 6-π-Systeme." Zeitschrift für Chemie 7, no. 6 (September 2, 2010): 209–16. http://dx.doi.org/10.1002/zfch.19670070602.

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7

Hoffmann, Siegfried, Werner Witkowski, and Hermann Schubert. "Nucleinsäuremodelle; 2-Pyridon-Systeme." Zeitschrift für Chemie 14, no. 4 (September 1, 2010): 154. http://dx.doi.org/10.1002/zfch.19740140409.

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8

Hellwinkel, Dieter, and Helmut Fritsch. "Phenylvinylog erweiterte Triphenylmethylium-Systeme." Chemische Berichte 122, no. 12 (December 1989): 2351–59. http://dx.doi.org/10.1002/cber.19891221223.

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9

Hellwinkel, Dieter, and Helmut Fritsch. "Phenylazo-substituierte Triphenylmethylium-Systeme." Chemische Berichte 123, no. 11 (November 1990): 2207–26. http://dx.doi.org/10.1002/cber.19901231120.

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10

Thoss, Michael. "Quantendynamik komplexer Systeme." Nachrichten aus der Chemie 56, no. 3 (March 2008): 327–30. http://dx.doi.org/10.1002/nadc.200853307.

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11

Jochum, Christian. "Integrierte Management-Systeme." Chemie Ingenieur Technik - CIT 69, no. 6 (June 1997): 799–800. http://dx.doi.org/10.1002/cite.330690606.

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12

Rähse, W. "Produktdesign disperser Systeme." Chemie Ingenieur Technik 80, no. 9 (September 2008): 1418–19. http://dx.doi.org/10.1002/cite.200750454.

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13

Böcker, S., and G. Ronge. "Destillation viskoser Systeme." Chemie Ingenieur Technik 76, no. 12 (February 6, 2004): 102–6. http://dx.doi.org/10.1002/cite.200403297.

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14

Clever, Guido. "Schaltbare Wirt-Gast-Systeme." Nachrichten aus der Chemie 63, no. 10 (October 2015): 995–98. http://dx.doi.org/10.1002/nadc.201590352.

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15

Hinrichs, Winfried, Peer Berges, and Günter Klar. "Selbststapelnde Systeme, IV 2,3,7,8-Tetramethoxythianthreniumsalze/Selfstacking Systems, Part IV 2.3.7.8-Tetramethoxythianthrenium Salts." Zeitschrift für Naturforschung B 42, no. 2 (February 1, 1987): 169–76. http://dx.doi.org/10.1515/znb-1987-0209.

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Abstract:

Abstract By addition of solutions of nitrosyl hexachloroantimonate(V) in acetonitrile or of diiodine in n-hexane to a solution of 2.3.7.8-tetramethoxythianthrene (“Vn2S2”, 1) in toluene the oxidation products [Vn2S2][SbCl6] • CH3CN (2) and [Vn2S2]I3 (3), resp., are formed. Crystal structure determinations show both compounds to contain the [Vn2S2]+ ion. In contrast to the folded parent compound Vn2S2 its monocation [Vn2S2] T is planar, the short CS and CO distances (172-173 pm and 134-135 pm resp.) indicate an extended mesomeric system. Both compounds crystallize with segregated stacks of cations and anions. In 2 the coplanarly and equidistantly stacked [Vn2S2]+ ions have an A,B-sequence (distance between the planes of the ions 353 pm, intermolecular S···S distance 366 pm). In 3 the [Vn2S2]+ ions form dimers by SS contacts (S···S distance 316 pm); these dimers are arranged in a stair-like manner (distances between atoms of adjacent dimers 350-380 pm). The conductivities of 2 and 3 are 9.4 • 10-9 and 5.3 • 10-6 Sem-1 , resp.

16

Fournival, J. L., J. C. Rouland, and R. Ceolin. "Le systeme EAU-phenobarbital." Journal of Thermal Analysis 34, no. 1 (January 1988): 161–75. http://dx.doi.org/10.1007/bf01913382.

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17

Rouland, J. C., J. L. Fournival, and R. Ceolin. "Le systeme eau-theophylline." Journal of Thermal Analysis 35, no. 5 (September 1989): 1643–49. http://dx.doi.org/10.1007/bf01912939.

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18

Grote, Leni, Gisela Riesel, and Hans-Joachim Bittrich. "Mischungsenthalpien binärer Systeme mit Dimethylformamid (DMFA)." Zeitschrift für Chemie 7, no. 11 (September 2, 2010): 444. http://dx.doi.org/10.1002/zfch.19670071132.

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19

Bestmann, Hans J�rgen, and Otto Vostrowsky. "Chemische Informations-systeme der Natur: Insektenpheromone." Chemie in unserer Zeit 27, no. 3 (July 1993): 123–33. http://dx.doi.org/10.1002/ciuz.19930270304.

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20

Hennig, Horst, Frank Dietze, Philipp Thomas, and Detlef Rehorek. "Photokatalytische Systeme; Heterocyclische Endiole als Metallchelatbildner." Zeitschrift für Chemie 18, no. 12 (August 31, 2010): 458–60. http://dx.doi.org/10.1002/zfch.19780181212.

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21

Bartels, Klaus. "Universeller elektrochemischer Detektor für fließende Systeme." Zeitschrift für Chemie 30, no. 11 (August 31, 2010): 419. http://dx.doi.org/10.1002/zfch.19900301118.

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22

Lisdat, Fred, Werner Moritz, and Lothar Müller. "Referenzelektroden für wäßrige und geschmolzene Systeme." Zeitschrift für Chemie 30, no. 12 (August 31, 2010): 427–33. http://dx.doi.org/10.1002/zfch.19900301203.

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23

Maier, Günther, Jörg Glatthaar, and Hans Peter Reisenauer. "Hetero-π-Systeme, 17: Aminosilylen (Aminosilandiyl)." Chemische Berichte 122, no. 12 (December 1989): 2403–5. http://dx.doi.org/10.1002/cber.19891221231.

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24

Koers, J. H., and F. E. C. Scheffer. "Beitrag zur Kenntnis Binärer Systeme. II." Recueil des Travaux Chimiques des Pays-Bas 49, no. 10 (September 3, 2010): 915–54. http://dx.doi.org/10.1002/recl.19300491003.

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25

Koers, J. H., and F. E. C. Scheffer. "Beitrag zur Kenntnis Binärer Systeme. IV." Recueil des Travaux Chimiques des Pays-Bas 53, no. 3 (September 3, 2010): 279–87. http://dx.doi.org/10.1002/recl.19340530311.

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26

Berger, Robert. "Gebrochene Symmetrie und molekulare Systeme." Nachrichten aus der Chemie 57, no. 2 (February 2009): 132–36. http://dx.doi.org/10.1002/nadc.200963606.

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27

Thiel, Walter. "Komplexe chemische Systeme realistisch modellieren." Nachrichten aus der Chemie 61, no. 11 (November 2013): 1095–96. http://dx.doi.org/10.1002/nadc.201390355.

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28

Marquardt, Rüdiger, Paul Präve, and Ernst Ludwig Winnacker. "Gezielte Nutzung biologischer Systeme." Chemie Ingenieur Technik 59, no. 1 (January 1987): 27–34. http://dx.doi.org/10.1002/cite.330590106.

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29

Grobe, Joseph, and Duc Le Van. "Reaktive EC (p-p)π-systeme." Journal of Organometallic Chemistry 311, no. 1-2 (September 1986): 37–43. http://dx.doi.org/10.1016/0022-328x(86)80216-9.

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30

Grobe, Joseph, Duc Le Van, Wolfgang Meyring, Bernt Krebs, and Mechthild Dartmann. "Reaktive EC (pp)π-Systeme." Journal of Organometallic Chemistry 340, no. 2 (February 1988): 143–51. http://dx.doi.org/10.1016/0022-328x(88)80070-6.

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31

Grobe, Joseph, Duc Le Van, and Joachim Welzel. "Reaktive EC (pp) π-Systeme." Journal of Organometallic Chemistry 340, no. 2 (February 1988): 153–60. http://dx.doi.org/10.1016/0022-328x(88)80071-8.

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32

Grobe, Joseph, Duc Le Van, Wolfgang Meyring, Bernt Krebs, and Mechtild Dartmann. "Reaktive EC (pp) π-Systeme." Journal of Organometallic Chemistry 346, no. 3 (June 1988): 361–77. http://dx.doi.org/10.1016/0022-328x(88)80137-2.

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33

Grobe, Joseph, Jürgen Szameitat, and Manfred Möller. "Reaktive EC (pp) τ-systeme." Journal of Organometallic Chemistry 344, no. 1 (April 1988): 61–69. http://dx.doi.org/10.1016/0022-328x(88)80213-4.

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34

Grobe, Joseph, Duc Le Van, Bernt Krebs, Mechtild Dartmann, F. Gordon, A. Stone, and Jürgen Szameitat. "Reaktive EC (p—p) π-Systeme." Journal of Organometallic Chemistry 399, no. 1-2 (December 1990): 189–98. http://dx.doi.org/10.1016/0022-328x(90)80096-i.

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35

Wobst, Michael, Gerd Hradetzky, Hans-Joachim Bittrich, and Vladimír Dohnal. "Grenzaktivitätskoeffizienten binärer ethylacetat-kohlenwasserstoff-systeme mit der kinetischen mitführung und der differentialebulliometrie." Collection of Czechoslovak Chemical Communications 52, no. 10 (1987): 2359–64. http://dx.doi.org/10.1135/cccc19872359.

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Abstract:

Unter bestimmten Bedingungen sind sowohl die kinetische Mitführung als auch die Differentialebulliometrie für Messungen bei der Grenzaktivitätskoeffizienten binarer Systems geeignet. Solche Messungen wurden für 4 binäre Systeme Ethylacetat-Kohlenwasserstoff bei 338,15 K durchgeführt. Die Ergebnisse beider Methoden stimmen sehr gut überein. für die kinetische Mitführung wird der Einfluss des Realverhaltens der Gasphase diskutiert.

36

Trzebiatowski, W., and R. Horyń. "Phasengleichgewichte einiger binärer Systeme, die Scandiumoxid enthalten." Zeitschrift für Chemie 5, no. 9 (September 2, 2010): 347. http://dx.doi.org/10.1002/zfch.19650050913.

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37

Rambusch, Torsten, Kerstin Hollmann-Gloe, and Karsten Gloe. "Molecular Modeling-Studien schwefelhaltiger Wirt/Gast-Systeme." Journal für praktische Chemie 341, no. 3 (April 1999): 202–17. http://dx.doi.org/10.1002/(sici)1521-3897(199904)341:3<202::aid-prac202>3.0.co;2-a.

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38

Maier, Günther, Norbert Hermann Wiegand, Stefan Baum, and Reinhold Wüllner. "Valenzisomerisierungen, 180 Valenzisomerisierungen persubstituierter (CH)10-Systeme." Chemische Berichte 122, no. 4 (April 1989): 781–94. http://dx.doi.org/10.1002/cber.19891220427.

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39

Fournival, J. L., R. Ceolin, J. C. Rouland, P. Toffoli, P. Khodadad, and J. Astoin. "Le systeme L-citrulline-eau." Journal of Thermal Analysis 32, no. 1 (January 1987): 213–25. http://dx.doi.org/10.1007/bf01914563.

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40

Sismondi, A., S. Szönyi, P. Abenin, L. Joncheray, and A. Cambon. "Neue Substanzen zur Herstellung vesikulärer Systeme / New Agents for Vesicular Systems." Tenside Surfactants Detergents 29, no. 3 (May 1, 1992): 166–68. http://dx.doi.org/10.1515/tsd-1992-290308.

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41

Pröbster, Manfred. "Welche Systeme stehen im Wettbewerb?" adhäsion KLEBEN & DICHTEN 54, no. 7-8 (July 2010): 34–39. http://dx.doi.org/10.1007/bf03243929.

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42

Gross, Ursula, and Heinz Blenke. "Eine Gasliftkaskade für fluide Systeme." Chemie Ingenieur Technik 61, no. 6 (June 30, 1989): 476–77. http://dx.doi.org/10.1002/cite.330610609.

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43

Ahrens, W. "CAE-Systeme für die Prozeßleittechnik." Chemie Ingenieur Technik 69, no. 9 (September 1997): 1236–37. http://dx.doi.org/10.1002/cite.330690930.

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44

Ahrens, Wolfgang. "CAE-Systeme für die Prozeßleittechnik." Chemie Ingenieur Technik 70, no. 5 (May 1998): 499–507. http://dx.doi.org/10.1002/cite.330700503.

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45

Burschka, A., and O. Molerus. "29. Beobachtung bewegter disperer Systeme." Chemie Ingenieur Technik 65, no. 9 (September 1993): 1065–66. http://dx.doi.org/10.1002/cite.330650931.

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46

Delgado, A., W. Kowalczyl, A. Baars, M. Breuer, and Ö. Ertunc. "Partikuläre Systeme in der Mikrofluidik." Chemie Ingenieur Technik 79, no. 9 (September 2007): 1382. http://dx.doi.org/10.1002/cite.200750414.

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47

Ищенко and A. Ishchenko. "To the question about the necessity of descriptive geometry and graphics teaching for chemists and chemistry technologists." Geometry & Graphics 1, no. 2 (July 25, 2013): 6–7. http://dx.doi.org/10.12737/776.

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Abstract:

The vital necessity of descriptive geometry and graphic study by students which are training in the specialties of chemist and chemistry technologist is shown. It is concluded that any engineering and scientific creativity in modern chemistry as the science of materials, structural chemistry and chemical dynamics of molecular systems’ interaction process is impossible without the foundations of descriptive geometry, which forms and develops the human spatial thinking. The discovery of conformational transitions in molecules and, in the future, conformational analysis, has predetermined the broad use of descriptive geometry methods in the chemical science. The modern chemistry’s state analysis is leading to conclusion that at present time the descriptive geometry is needed in the educational program of modern chemist and chemistry technologist.

48

Szönyi, F., and A. Cambon. "Neue Substanzen zur Herstellung micro-dispenser Systeme / Novel Agents for Microdispersed Systems." Tenside Surfactants Detergents 31, no. 2 (March 1, 1994): 124–27. http://dx.doi.org/10.1515/tsd-1994-310221.

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49

Morgant, G., and B. Legendre. "Etude du systeme binaire selenium-tellure." Journal of Thermal Analysis 31, no. 2 (March 1986): 377–85. http://dx.doi.org/10.1007/bf01911070.

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50

Zimmermann, K., C. Pasel, M. Luckas, and J. ‐D Herbell. "Löslichkeit von Schwefeldioxid in wässrigen Systemen bei höheren Elektrolytkonzentrationen – I. Chloridhaltige Systeme." Chemie Ingenieur Technik 80, no. 7 (July 2008): 987–95. http://dx.doi.org/10.1002/cite.200800003.

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