ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 6 (1992), S. 69-74 
    ISSN: 0268-2605
    Keywords: Estertin complexes ; S-benzyldithio-carbazate ; Schiff bases ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Schiff bases [H2SBSaD], [H2SBVD] and [H2SBND], derived by the condensation of S-benzyldithiocarbazate and salicylaldehyde, 2-hydroxy-3-methoxybenzaldehyde and 2-hydroxy-1-naphthaldehyde respectively, react with diestertin dichlorides, R2SnCl2 [R=—CH2CH2CO2CH3, —CH2CH2CO2C2H5 or —CH2CH2CO2C4H9] in 1:1 molar proportion to yield chlorine-substituted complexes of the type R2Sn(Schiff base), the base being tridentate. The complexes are characterized on the basis of their elemental analyses, IR and 1H NMR spectral studies. The 13C and 119Sn NMR and the tin-carbon coupling constant data reveal the structures of the complexes to be octahedral with trans ester grouping, and bidentate ester linkages. The pentacoordinated complex (CH3)2Sn(SBSaD) was prepared by the reaction of dimethyltin oxide with H2SBSaD in equimolar proportions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 7 (1993), S. 63-69 
    ISSN: 0268-2605
    Keywords: Organotin Schiff base complexes ; spectroscopic studies ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organotin(IV) Schiff base complexes of the type (L)SnR2 [where R=CH3, C6H5 or CH2CH2CO2 CH3], (LH)Sn(C6H5)3 and (L)SnCl(CH2CH2CO2 CH3) [where LH2=2-N-salicylideneimino-2-methyl-1-propanol, derived from the condensation of salicylaldehyde and 2-amino-2-methyl-1-propanol] have been prepared and characterized on the basis of their elemental analyses, IR, 1H, 13C and 119Sn NMR studies. In these mononuclear complexes the Schiff base acts either as a dianionic tridentate or as a monobasic bidentate moiety by coordinating through an alkoxy group, an azomethine nitrogen and a phenoxide ion to tin. Sulphur dioxide inserts in the tin-methyl/-phenyl bond in the above Schiff base complexes to give tin-O-sulphinates of formulae (L)RSn(SO2R) and (LH)(C6H5)2Sn(SO2C6H5).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 465 (1980), S. 204-208 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Neue Chelate des Bis-β- Carbomethoxyethlzinn(IV)Zwei- und dreizähnige Chelatinganden (s. Abstract) Können die Chloratome des Bis-β-carbomethoxethyldichlozinn(IV) unter Bildung neuer stabiler Chelatverbindungen ersetzen. Bromierung dieser Verbindungen unter milden Bedingungen zeigt, daß die Chelatinganden bevorzugt abgespalten werden. Die neun Verbindungen werden durch Elementaranalyse, IR- und PMR-Spektren sowie Molekulargewichtsbestimmungen Charakterisiert und mögliche Strukturen werden Vorgeschlagen.
    Notes: Bi- and tri-denate Chelating ligands (acetylacetone, salicylasehyde, 8-hydroxy quinoline, dibenzoylmethane, benzoyl phenhydroxlmanine, 2-hydroxy benzophenone, 2-hydroxy 4-methoxy benzophenone and salichyaldine) replace cholrine atoms of bis-β-carbomethoxyethyl dischlorotin (IV) to form new stable Cheleted compounds. Bromination studies under mild conditions indicate that in these compounds the Cheleated ligand part is preferentially cleaved. The new compounds are characterized by elemental analysis. IR and PMR spectra and molecular weight, and possible structures have been assigned.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 527 (1985), S. 203-207 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kationische Carbonyl-Ruthenium(II)-Komplexe mit Nitril-LigandenStabile kationische Komplexe vom Typ [RuCO(PPh3)2(L)RCN]+[ClO4]-, mit Acetonitril bzw. Acrylonitril wurden dargestellt. Als zweizähnige Liganden (LH) dienten Acetylaceton, Benzoylaceton, Dibenzoylmethan, Trifluorothenoylaceton und 8-Hydroxochinolin. Die Komplexe wurden analysiert, ferner durch IR-, 1H- und 31P-NMR-, Leitfähigkeits- und ESCA-Messungen charakterisiert; eine Stereochemie erscheint möglich.
    Notes: Stable cationic complexes of the type [RuCO(PPh3)2(L)(RCN)]+[ClO4]- derived from acetonitrile and acrylonitrile have been synthesized. The bidentate ligands (LH) used are acetylacetone, benzoylacetone, dibenzoylmethane, trifluorothenoyl acetone and 8-hydroxyquinoline. The complexes have been characterized by elemental analysis, IR, conductivity, 1H and 31P NMR and ESCA studies, and possible stereochemistry has been established.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 536 (1986), S. 173-178 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Schiffsche Basen-Komplexe des Rhodium(I) mit dreizähnigen N-Methyl-S-methyldithiocarbazat-LigandenSchiffsche Basen aus der Kondensation von β-Diketonen mit N-Methyl-S-methyl-dithiocarbazaten ergeben bei Reaktion mit [Rh(μ-Cl)(CO)2]2 cis-Dicarbonyl-Komplexe Rh(CO)2(Schiff). Die aus aromatischen Aldehyden erhaltenen bilden trans-Dicarbonyl-Komplexe. Mit einem Überschuß von Triphenylphosphin ergeben diese Komplexe nur Rh(CO)(PPh3)(Schiff). Cis-1,5-cyclooctadien (COD) reagiert mit cis-Dicarbonyl-Komplexen zu carbonylfreien Produkten Rh(COD)(Schiff); gleiche Reaktionen wurden bei trans-Dicarbonyl-Komplexen beobachtet. Oxydative Addition von Brom an diese Komplexe ergibt Dibromderivate, in denen die Schiffsche Base als zweizähniger Ligand wirkt, Rh(PPH3)2(Schiff)-Komplexe wurden durch Reaktion oben genannter Schiffscher Basen mit Rh(PPh3)3Cl erhalten. Die Strukturen dieser neuen Komplexe wurden auf Grund von IR-und 1H-NMR-Spektren bestimmt.
    Notes: Schiff bases derived from the condensation of β-diketones with N-methyl-S-methyldithiocarbazates yield cis dicarbonyl complexes Rh(CO)2 (Schiff) on reaction with [Rh(μ-Cl)(CO)2]2. Those derived from aromatic aldehydes form trans dicarbonyl complexes. These complexes with excess of triphenylphosphine give only Rh(CO)(PPh3)(Schiff). cis-1,5-cyclooctadiene (COD) reacts with cis dicarbonyl complexes to yield the carbonyl-free product Rh(COD)(Schiff); similar reactions have not been observed in the case of trans-dicarbonyl complexes. Oxidative addition of bromine to these complexes yields dibromo derivative in which the Schiff base acts as bidentate chelate. Rh(PPh3)2(Schiff) complexes have been obtained from the reaction of above Schiff bases with Rh(PPh3)3Cl. The structures of these new complexes have been determined based on IR and 1H NMR spectra.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 1986-05-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 1980-06-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 1985-08-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 154 (1993), S. 101-112 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Calcium plays a crucial role in regulating the growth and differentiation of cultured keratinocytes. However, the mechanism(s) of this regulation is not clear. Prior studies have shown that intracellular free calcium (Cai) increases with keratinocyte differentiation. In this study, in order to evaluate the role of cytosolic free calcium and organelle-bound calcium in keratinocyte differentiation, we quantitated and localized calcium pools in keratinocytes, utilizing the fluorescence probe indo-1 and ion-capture cytochemistry, respectively. Cai of undifferentiated keratinocytes was 80-120 nM, whereas Cai of differentiated keratinocytes was 200-300 nM depending on the extent of differentiation. The Cai of individual cells in an undifferentiated colony was heterogeneous (60-160 nM) with larger cells displaying higher Cai. Heterogeneity also was observed in the intracellular calcium-containing precipitates in the different layers of stratifying keratinocyte cultures using the cytochemical technique. Calcium precipitates were abundant in the lower cell layers, progressively decreasing apically, with the uppermost layer devoid of precipitates. Calcium-containing precipitates appeared as fine-tocoarse electron-dense granules on the plasma membrane, within the cytosol, mitochondria, nucleus, and vacuolar organelles. Whereas ionomycin in the presence of extracellular calcium increased the amount of intracellular calcium precipitates, EGTA removed calcium precipitates from organelles. Unlike intact epidermis, keratinocytes displayed no extracellular calcium reservoirs. Putative calcium binding sites, visualized by trivalent lanthanum (La) binding, were abundant on cell membranes and desmosomes of basaloid cells, but decreased in the upper cell layers. These studies revealed differences in the distribution of free ionic calcium (as determined by the fluorescence technique) and organelle-bound calcium (as determined by the cytochemical technique). Striking differences were also observed in calcium localization between intact epidermis and cultured epidermal cells. The localization pattern of calcium in cultured keratinocytes may reflect the hyperproliferative state of these cells, as in psoriatic epidermis, and/or the absence of a normal permeability barrier in these submerged cultures. © 1993 Wiley-Liss, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 37 (1990), S. 685-699 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Earlier definitions of valencies of atoms, molecules, and molecular orbitals are extended to configuration interaction (CI) wave functions. Using these definitions, valencies both at equilibrium and nonequilibrium geometries of molecules are calculated at the CI level and compared with non-CI results. CI valency correlation diagrams are obtained. Valency variation with bond length using correlated wave functions is found to behave properly unlike in the case of SCF wave functions.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...