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  • Inorganic Chemistry  (38)
  • Lunar and Planetary Science and Exploration  (10)
  • Condensed Matter: Electronic Properties, etc.  (3)
  • Chaperone  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Glycosylation inhibits the interaction of invertase with the chaperone GroEL
    Amsterdam : Elsevier
    FEBS Letters 305 (1992), S. 203-205 
    Details
    ISSN: 0014-5793
    Keywords: Aggregation ; Chaperone ; Folding ; Glycosylation ; GroE ; Invertase
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/0014-5793(92)80667-6
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  • 2
    Electronic Resource
    Electronic Resource
    Comparison of the expression of a plastidic chaperonin 60 in different plant tissues and under photosynthetic and non-photosynthetic conditions (1996)
    Springer
    Planta 200 (1996), S. 326-334 
    Details
    ISSN: 1432-2048
    Keywords: Chaperone ; Chloroplasts ; Chromoplasts ; Heat-shock protein ; Secale
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A partial cDNA which codes for the β-subunit of a plastidic chaperonin 60 (cpn60-β) from rye (Secale cereale L.) leaves was identified and sequenced, except for 46 amino acids of the N-terminus of the mature protein and the transit sequence. This is the first cpn60-β sequence determined for a monocotyledonous plant. Specific antibodies against cpn60-β were affinity-purified from an antiserum raised against the total soluble protein fraction of ribosome-deficient plastids. The localization of cpn60-β in chloroplasts or non-green plastids was confirmed by immunodetection in Percoll gradient-purified organelles. The expression and occurrence of cpn60-β was analysed by immunoblotting with the specific antibodies and Northern hybridization. The cpn60-β protein was constitutively expressed in various green and non-green tissues. It was evenly distributed along the major part of a rye leaf, while highest transcript levels occurred in the youngest and oldest leaf sections. The expression of the cpn60-β protein was not enhanced by a heat-shock treatment at 42 °C. The cpn60-β transcript and protein were more strongly expressed in various non-green, for instance etiolated, 70S-ribosome-deficient 32 °C-grown, or herbicide-bleached tissues, than in green leaves of rye. A rapid increase in the cpn60-β transcript level was also observed when green leaves were transferred from light to darkness while the protein level was not affected. The dark-induced increase in the cpn60-β transcript was totally suppressed in the presence of 2% sucrose. Inhibitor treatments suggested that the change in cpn60-β transcript level was not related to changes of the ATP supply of the tissue. While the large subunit of the photosynthetic protein ribulose-1,5-bisphosphate carboxylase was largely degraded during ripening of tomato fruits, high levels of cpn60-β were detected in tomato chromoplasts and in the yellow flower petals of Narcissus. Low levels of cpn60-β were detected in root tissue.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00200300
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  • 3
    Electronic Resource
    Electronic Resource
    Zur präparativen Reindarstellung von pentamerem ThioformaldehydFrau Professor Margot Becke-Goehring zum 60. Geburtstage gewidmet (1974)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 406 (1974), S. 271-276 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation of Pure Pentameric ThioformaldehydeThe different behaviour of the Trithiane- and Pentathiecane-silver-complex compounds may be used for the preparation of pure (CH2S)5.
    Notes: Das unterschiedliche Verhalten der Silberkomplexe von Trithian und Pentathiecan läßt sich zur präparativen Reindarstellung von (CH2S)5 ausnützen.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19744060220
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  • 4
    Electronic Resource
    Electronic Resource
    Zur Kenntnis von nur im festen Zustand existenzfähigen 1:1-Verbindungen zwischen Antimon(III)-Halogeniden und 1,3,5-Trithiacyclohexan (s-Trithian) (1977)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 437 (1977), S. 149-154 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Characterization of Weak Bonded Solid 1:1 Adducts Formed between Antimony(III) Halogenides and s-TrithianeCrystalline 1:1 addition compounds are formed on cooling hot solutions of antimony(III) halides and s-trithiane in benzene or toluene. Their preparation, physical properties and vibrational spectra are described.
    Notes: Aus den Gemischen heißer Lösungen von s-Trithian und Antimon(III)-Halogeniden in Benzol oder Toluol kristallisieren beim Erkalten 1:1-Additionsverbindungen. Ihre Darstellung, physikalischen Eigenschaften und Schwingungsspektren werden beschrieben.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19774370119
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  • 5
    Electronic Resource
    Electronic Resource
    Zum nukleophilen Abbau von Tris(pentasulfido)platinat(IV), [Pt(S5)3]2-, und Bis(pentasulfido)platinat(II),[Pt(S5)2]2- (1979)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 452 (1979), S. 112-122 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Nucleophilic Degradation of Tris(pentasulfido)platinum(IV), [Pt(S5)3]2-, and Bis(pentasulfido)platinum(II), [Pt(S5)2]2-The behaviour of [Pt(S5)3]2-, (I), towards sulfite, arsenite, sulfide, hydroxide, and triphenylphosphine has been studied qualitatively and quantitatively. With stoichiometric amounts of nucleophile one ring is degraded; the reaction product [Pt(S5)2]2-, (II), can be isolated. With excess of nucleophile all sulfur atoms are taken off from the platinum; with triphenylphosphine, however, (PPh3)2PtS4, (III), is formed. A mechanistic interpretation of the course of the reaction is given and supported by kinetic studies.
    Notes: Das Verhalten von [Pt(S5)3]2-, (I), gegenüber Sulfit, Arsenit, Sulfid, Hydroxid und Triphenylphosphin wird qualitativ und quantitativ untersucht. Mit stöchiometrischen Mengen an Nukleophil wird ein Ring abgebaut; als Reaktionsprodukt kann [Pt(S5)2]2-, (II), isoliert werden. Mit Überschuß an Nukleophil werden alle Schwefelatome vom Platin abgelöst; mit Triphenylphosphin entsteht dagegen (PPh3)2PtS4, (III). Der Reaktionsablauf wird mechanistisch gedeutet und durch kinetische Untersuchungen erhärtet.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19794520116
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  • 6
    Electronic Resource
    Electronic Resource
    Acyl- und Alkylidenphosphane. XXXII [1, 2]. Di-cyclo-hexoyl- und Diadamant-1-oylphosphan  -  Keto-Enol-Tautomerie und Struktur (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 608 (1992), S. 33-42 
    Details
    ISSN: 0044-2313
    Keywords: Diacylphosphines ; Di-cyclohexoylposphine ; Diadamant-1-oylphosphine ; keto-enol tautomerism ; NMR-parameters, thermodynamic data ; X-ray structure determination ; very short O‥H‥O bridge ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Acyl- and Alkylidenephosphines. XXXII. Di-cyclohexoyl- and Diadamant-1-oylphosphine - Keto-Enol Tautomerism and StructureLithium dihydrogenphosphide · DME (1) [12] and cyclo-hexoyl or adamant-1-oyl chloride react in a molar ratio of 3:2 to give lithium di-cyclo-hexoylphosphide · DME and the corresponding diadamant-1-oylphosphide.2THF (1) resp. Treatment of these two compounds with 85% tetrafluoroboric acid. diethylether adduct yields di-cyclo-hexoyl- (1b) and diadamant-1-oylphosphine (1c). In nmr spectroscopic studies 1b over a range of 203 to 343 K, a strong temperature dependence of the keto-enol equilibrium is found; thermodynamic data characteristic for the formation of the enol tautomer (ΔH0 = -4.3 kJ. mol-1; ΔS0 = -9.2 J. mol-1. K (-1) are compared of 1,3-diketones.The enol tautomer of diadamant-1-oylphosphine (E-1c) as obtained from a benzene solution in thin colourless plates, crystallizes in the monoclinic space group P21/c {a = 722.2(2); b = 1085.5(4); c = 2434.8(5) pm; ß = 96.43(2)° at -100 ± 3°C; Z = 4}. An X- ray structure analysis (Rw = 0.033) shows bond lengths and angles to be almost identical within the enolic system (P—C 179/180; C—O 130/129; C—C(adamant-1-yl) 152/153 pm; C—P—C 99°; P—C—O 124°/124°; P—C—C 120°/120°; C—C—O 116°/116°. The geometry of the very strong, but probably asymmetric O‥H‥O bridge is discussed (O—H 120/130, O‥O 245 pm).
    Notes: Aus Lithium-dihydrogenphosphid · DME (1) [12] und cyclo-Hexoyl- bzw. Adamant-1-oyl-chlorid im Molverhältnis 3:2 zugängliches Lithium-di-cyclo-hexoylphosphid · DME und -diadamant-1-oylphosphid · 2THF 1) reagieren mit 85proz. Tetrafluoroborsäure · Diethylether-Addukt zu Di-cyclo-hexoyl- 1b) und Diadamant-1-oylphosphan (1 c). Die Lage des Keto-Enol-Gleichgewichts zwischen 203 und 343 K sowie thermodynamische Daten zur Bildung des Enol-Isomers ΔH0= -4,3kJ.Mol-1; ΔS0;=-9,2 J · mol-1 · K-1 () wurden NMR-spektroskopisch an einer 2 M Lösung des bei +20°C flüssigen Di-cyclo-Hexoyl-Derivates 1b in d8-Toluol ermittelt und mit Werten von 1,3-Diketonen verglichen.Das farblose, sich aus Benzol in dünnen Plättchen abscheidende Enol-Tautomer des Diadamant-1-oylphosphans (E-1 c) kristallisiert monoklin in der Raumgruppe P21/c {a = 722,2(2) b = 1085,5(4); c = 2434,8(5) pm; ß = 96,43(2)° bei - 100 ± 3°C; Z = 4}. Nach den Ergebnissen der Röntgenstrukturanalyse (Rw=0,033) weist das Molekül in beiden des Hälften des Enolrings nahezu identische Bindungslängen und -winkel auf P—C 179/180; C—O 130/129; C—C(Adamant-1-yl) 152/153 pm; C—P—C 99°; P—C—O 124°/124°; P—C—C 120°/120°; C—C—O 116°/116°. Die Geometrie der sehr starken, aber vermutlich asymmetrischen O‥H‥O-Brücke wird diskutiert (O—H 120/130; O‥O 245 pm).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926080206
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  • 7
    Electronic Resource
    Electronic Resource
    Cycloaddition von Benzothiet an 4-substituierte Styrole (1989)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 2209-2209 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19891221125
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  • 8
    Electronic Resource
    Electronic Resource
    Zur Identität der aus Thioschwefelsäure mit Dichlordisulfan und aus Thioschwefelsäure mit salpetriger Säure hergestellten Tetrasulfandisulfonate und zur Existenz eines „Saueren“ Tetrasulfan-disulfonats (1964)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 330 (1964), S. 179-187 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The product prepared following the method of GOEHRING and FELDMANN from H2S2O3 and S2Cl2 is not a „spectrum“ of different salts as stated by WEITZ and BECKER, but really K2S6O6, which is also prepared from H2S2O3 and HNO2. Tetrasulfane-disulfonate does not only exist in the neutral form K2S6O6, but also in a „acid“ form with a part of the potassium - nonstoichiometrically - replaced by H+. The two forms have different shape and X-ray spectra.
    Notes: Bei dem nach GOEHRING und FELDMANN aus H2S2O3 und S2Cl2 dargestellten Produkt handelt es sich nicht, wie von WEITZ und BECKER angegeben, um ein „Spektrum“ verschiedener Salze, sondern um einheitliches K2S6O6, wie es auch aus H2S2O3 und HNO2 erhalten wird. Tetrasulfan-disulfonat existiert neben der neutralen Form K2S6O6 noch in einer „saueren“ Form, bei der ein Teil des Kaliums - nichtstöchiometrisch - durch H+ ersetzt ist. Die beiden Formen unterscheiden sich in Aussehen und Röntgenspektrum voneinander.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19643300310
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  • 9
    Electronic Resource
    Electronic Resource
    Versuche zur Trennung von Sulfan-disulfonaten mit Hilfe von Anionenaustauschern (1964)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 330 (1964), S. 188-194 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The separation of sulfane-disulfonates, sulfite and thiosulfate by anion-exchangers has been studied. Whereas K2S6O6 is decomposed on the column, the salts K2S3O6, K2S4O6 and K2S5O6 may be separated quantitatively.
    Notes: Die Trennung von Sulfan-disulfonaten, Sulfit und Thiosulfat mit Anionenaustauschern wird untersucht. Während K2S6O6 auf der Säule zu rasch zerfällt, lassen sich die Salze K2S3O6, K2S4O6 und K2S5O6 quantitativ voneinander trennen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19643300311
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  • 10
    Electronic Resource
    Electronic Resource
    Bromalkylselenoborane (1970)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 377 (1970), S. 305-309 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Borontribromide and one or two equivalents of alkaneselenol react under formation of dibromo-alkylselene-boranes or monobromo-bis-alkylselenoboranes. From the reaction of selenophenole and BBr3 phenylborondibromide is formed.
    Notes: Bortribromid reagiert mit einem oder zwei Äquivalenten Alkanselenol zu Dibrommonoalkylselenoboranen Br2BSeR bzw. zu den instabilen Monobromdialkylselenoboranen BrB(SeR)2. Aus Selenophenol und BBr3 entsteht dagegen Phenylbordibromid.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19703770312
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