Abstract:A gloomy view of modern society based on the assumption that those in charge form a "cognitive élite" which is likely to be dynastic mischievously begs too many questions.
“…[2] and [ 3 ] originating from ground state levels with pair spin S as a function of temperature. The symbols denote experimental intensities determined from the absorption spectra in Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The solid lines are fits to eqs. [2] and [3] for the transitions originating from the ground state levels with pair spins S of 0 and 1, respectively, with a value of -295 cm-' for the exchange coupling parameter J in eq.…”
Section: Discussionmentioning
confidence: 99%
“…Binuclear complexes of iron and manganese with 0x0 and carboxylato bridging ligands are important constituents of the active sites in metalloproteins and have been shown to be catalytically active (1)(2)(3)(4)(5)(6). A large number of model compounds have been synthesized recently, among them a series of triply bridged binuclear compounds with the y-0x0-bis(y-acetato) bridging geometry (5,7).…”
Single-crystal absorption spectroscopy at variable temperature is used to determine exchange couplings between transition metal centers in both the electronic ground and excited states in two new homobimetallic complexes with the formula [LM(y-O)(y-CH3C02)2ML'](C104)2, where M is iron(II1) or manganese(II1).L and L' denote 1,4,7-triazacyclononane and 1,4,7-trimethyl-l,4,7-triazacyclononane, respectively. Values for the ground state exchange coupling constant J are -295 cm-I and +I0 cm-I for the iron and manganese compounds, respectively, using He, = -JS,.S,. Exchange interactions in excited states are qualitatively analyzed, indicating that a spin-forbidden transition of the Fe-Fe binuclear unit occurs with significant intensity by the single-ion mechanism, and not as expected by the Tanabe pair intensity mechanism for spin-forbidden transitions, the dominant mechanism for isoelectronic complexes of manganese(I1).
“…[2] and [ 3 ] originating from ground state levels with pair spin S as a function of temperature. The symbols denote experimental intensities determined from the absorption spectra in Fig.…”
Section: Discussionmentioning
confidence: 99%
“…The solid lines are fits to eqs. [2] and [3] for the transitions originating from the ground state levels with pair spins S of 0 and 1, respectively, with a value of -295 cm-' for the exchange coupling parameter J in eq.…”
Section: Discussionmentioning
confidence: 99%
“…Binuclear complexes of iron and manganese with 0x0 and carboxylato bridging ligands are important constituents of the active sites in metalloproteins and have been shown to be catalytically active (1)(2)(3)(4)(5)(6). A large number of model compounds have been synthesized recently, among them a series of triply bridged binuclear compounds with the y-0x0-bis(y-acetato) bridging geometry (5,7).…”
Single-crystal absorption spectroscopy at variable temperature is used to determine exchange couplings between transition metal centers in both the electronic ground and excited states in two new homobimetallic complexes with the formula [LM(y-O)(y-CH3C02)2ML'](C104)2, where M is iron(II1) or manganese(II1).L and L' denote 1,4,7-triazacyclononane and 1,4,7-trimethyl-l,4,7-triazacyclononane, respectively. Values for the ground state exchange coupling constant J are -295 cm-I and +I0 cm-I for the iron and manganese compounds, respectively, using He, = -JS,.S,. Exchange interactions in excited states are qualitatively analyzed, indicating that a spin-forbidden transition of the Fe-Fe binuclear unit occurs with significant intensity by the single-ion mechanism, and not as expected by the Tanabe pair intensity mechanism for spin-forbidden transitions, the dominant mechanism for isoelectronic complexes of manganese(I1).
“…1a, MnTACN) was the first bleach catalyst employed in commercial detergent products for the purpose of laundry cleaning (Favre et al 1991(Favre et al , 1993Hage et al 1994). The compound was first published in 1988 as a model for manganese-containing enzymes by Wieghardt and co-workers (Wieghardt et al 1988).…”
Section: Introductionmentioning
confidence: 99%
“…Generally, manganese containing compounds are preferred as possible catalysts in bleaching because of their environmental digestibility. Today, probably the most effective catalysts for stain oxidation by hydrogen peroxide at low temperatures are manganese complexes derived from 1,4,7-trimethyl-1,4,7-triazacyclononane and related ligand systems (Hage et al 1994;Hage and Lienke 2006). Up to now research on the application of these catalysts has mainly been done in detergent application and paper/pulp bleaching (Hage and Lienke 2006;Patt et al 1997), showing that the catalytic route can give improved stain removal and delignification.…”
Hydrogen peroxide can be catalyzed to bleach cotton fibers at temperatures as low as 308C by incorporating dinuclear tri-l-oxo bridged manganese(IV) complex of the ligand 1,4,7-trimethyl-1,4,7-triazacyclononane (MnTACN) as the catalyst in the bleaching solution. The catalytic system was found to be more selective under the conditions applied than the non-catalytic H 2 O 2 system, showing better bleaching performance while causing slightly lower decrease in degree of polymerization (DP) of cellulose. In order to gain fundamental knowledge of the bleach effect on cotton fibers and cellulose as its main component, especially after catalytic bleaching, X-ray Photoelectron Spectroscopy (XPS) was used to study surface chemical effects. The Washburn method was applied to investigate wetting properties, and liquid porosity was used to obtain pore volume distribution (PVD) plots. Parallel analyzes performed on model cotton fabric, i.e. ''clean'' cotton fabric stained with morin -a pigment regularly found in native cotton fiber, helped to differentiate between pigment oxidation and other bleaching effects produced on the (regular) industrially scoured cotton fabric. Bleaching was not limited to the chemical action but also affected cotton fiber capillary parameters most likely due to the removal of non-cellulosic materials as well as chain-shortened cellulose.
Das kovalente Verankern von 1,4‐Dimethyl‐1,4,7‐triazacyclononan an Kieselgel ist der erste Schritt bei der Herstellung eines heterogenisierten Mn‐Katalysators. Wird H2O2 als Oxidationsmittel eingesetzt, so kann das Material die vicinale cis‐Dihydroxylierung von disubstituierten Olefinen katalysieren, wie hier schematisch gezeigt ist. Dabei werden beide Enantiomere des Produkts erhalten.
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