Quecksilber(II)-Titrationen mit Variaminblau als Redoxindicator

Zusammenfassung Es wird eine volumetrische Methode zur Bestimmung von Cyanid- und Quecksilber(II)-ionen mit titrierter Quecksilber(II)-nitratlösung gegen Variaminblau als Indicator beschrieben. Das Verfahren liefert genaue, wenig streuende Werte.Vorgetragen auf der III. Arbeitstagung für analytische Chemie in Prag am 1. September 1959.     

Formation and reactions of metal-metal bonded heterobimetallic (C5H4PR2)-bridged (Zr-Ir) and (Zr-Rh) complexes: evidence for the participation of metal hydride intermediates

Treatment of the complexes [(C(5)H(4)PR(2))(2)Zr(CH(3))(2)](b: R = isopropyl; c: R = cyclohexyl) with the reagent HIr(CO)(PPh(3))(3) (2b) yield the heterobimetallic complexes [mu-C(5)H(4)PR(2))(2)(H(3)C-Zr-Ir(CO)(PPh(3)))] (4b, 4c) with evolution of methane. The reaction of the -PPh(2) substituted analogue with initially yields an intermediate [(H(3)C)(2)Zr(mu-C(5)H(4)PPh(2))(2)Ir(H)(CO)(PPh(3))] 5a, that still contains both methyl groups at zirconium and does not contain a metal-metal bond. At room temperature, the intermediate reacts further with methane formation to eventually yield the (Zr-Ir) complex 4a. The corresponding [mu-C(5)H(4)PR(2))(2)(H(3)C-Zr-Rh(CO)(PPh(3)))] complexes 3a (R = Ph) and 3b (R = isopropyl) react cleanly with isopropyl alcohol to liberate methane and yield the corresponding [mu-C(5)H(4)PR(2))(2)(Me(2)CHO-Zr-Rh(CO)(PPh(3)))] products (7a, 7b). Carefully monitoring the reaction of with Me(2)CHOH by NMR revealed that the Zr-Rh functionality is attacked first to give the intermediate [Me(Me(2)CHO)Zr([micro sign]-C(5)H(4)PR(2))(2)Rh(H)(CO)(PPh(3))] (6b). This intermediate then reacts further to cleave off methane and re-form the (Zr-Rh) metal-metal bond to yield the product 7b. The tetrametallic mu-oxo-(Zr-Rh) metallocene derivate 11a was obtained starting from the (Zr-Rh) complex 3a and it was characterized by X-ray diffraction. It may be that this reaction is also initiated by H-OH addition to the [Zr-Rh] metal-metal bond.     

ESR. Spectra and Structures of Radical Anions in the Dibenzo[a,e]cyclooctene Series

ESR. studies are reported for the radical anions of 5,6-didehydro- and 5,6,11,12-tetradehydro-dibenzo[a,e]cyclooctene (III and IV, resp.), in addition to that of dibenzo[a,e]cyclooctene (II) itself, the spectrum of which has been reexamined. Comparison of the proton and ¹³C coupling constants for II·?, III·? and IV·? indicates that the three radical anions do not differ greatly in their electronic and molecular structures. This statement implies that II·? should also be substantially planar, i.e., the tub-shaped eight-membered ring in II is expected to flatten on passing from the neutral molecule to its radical anion. Support for postulating such a change in geometry, analogous to that encountered with the parent cyclooctatetraene (I), is provided by INDO calculations.     

Elektronenreiche übergangsmetallkomplexe : II. Nitril-phosphan-molybdändicarbonyle: Farbe und solvatochromie

Complexes of aromatic or α,β-unsaturated nitriles YCN of the type (YCN)₂(PR₃)₂Mo(CO)₂ and (YCN)(PR₃)₃Mo(CO)₂ are new chromophores. Their intense electronic absorption band in the visible spectrum is strongly influenced by substituents and solvent polarity. Acceptor properties of nitriles are discussed on the basis of CNDO-calculations. CT-character and solvato-chromism can be interpreted in terms of the back-bonding ability of the nitriles in electron-rich metal complexes.     

ansa-Metallocene derivatives: VIII. Syntheses and crystal structures of ethylene-bridged titanocene and zirconocene derivatives with permethylated ring ligands

Ethylene-bridged titanocene and zirconocene derivatives with permethylated ring ligands, C₂H₄(C₅(CH₃)₄)₂TiCl₂ and C₂H₄(C₅(CH₃)₄)₂ZrCl₂, have been synthesized and their crystal structures determined.     

Bildung von 2-(1-Methyl-1, 4, 5, 6-tetrahydropyridyl-3)-2-oxazolin-4-on aus 1-Methyl-1, 4, 5, 6-tetrahydronicotinsäureamid und Bromessigsäureäthylester und seine Überführung in O-(1-Methylnipecotinoyl)glykolsäureamid via das dazu tautomere Cyclol

The main product of the reaction between 1-methyl-1, 4, 5, 6-tetrahydronicotin-amide and ethyl bromoacetate is shown to be the 2-(1-methyl-1, 4, 5, 6-tetrahydropyridyl-3)-2-oxazoline-4-one which on partial hydrogenation followed by reaction with alkali affords O-(1-methylnipecotinoyl)glycolic amide, presumably via the tautomeric cyclol.     

Heterotrimeric liquid crystalline thiadiazole derivatives

Abstract

Various trimeric co-oligomers combining 2-phenyl-1,3,4-thiadiazole mesogenic moieties with a biphenyl mesogenic moiety were synthesized and their mesomorphic behaviour investigated by polarizing microscopy, calorimetry and X-ray scattering. Such co-oligomeric structures provide an opportunity to combine different mesogenic units. Thus readily accessible homochiral biphenyl mesogenic units were connected with thiadiazole mesogenic units leading to an oligomeric liquid crystal material with ferroelectric properties.