Structural diversity and solution behavior of low-valent iridium complexes bearing 1,4-diazabutadiene ligands

Three types of 1,4-diazabutadiene stabilized low-valent iridium complexes, namely [IrCl(cod)(MesDAB)] (1), [IrCl(coe)(MesDAB)] (2) and [IrCl(MesDAB)₂] (3), have been prepared from 1,4-bis(2,4,6-trimethylphenyl)-1,4-diaza-1,3-butadiene (MesDAB) and [IrCl(cod)]₂ or [IrCl(coe)₂]₂, respectively. The complexes have been investigated by NMR spectroscopy and X-ray diffraction experiments. While tetra-coordinated 2 and penta-coordinated 3 maintain their solid state structure in solution, penta-coordinated 1 shows fluxional behavior. The crystal structures determined indicate strong π-backbonding towards the MesDAB ligand in all cases.     

Untersuchungen zur heterogenen Kondensation von Wasserdampf in Membrankontaktoren

Heterogeneous condensation can contribute to improve the separation efficiency of airborne particles. Submicron particles can be separated due to inertial impaction when particle mass is previously enlarged sufficiently by water vapor condensation. This paper presents a novel, membrane‐based process for creating the requisite supersaturation for condensation. The increase of the particle size based on vapor condensation is detected by a new inline measuring technique.     

In‐Depth Study of Mass Transfer in Nanoporous Materials by Micro‐Imaging

The first application of interference microscopy to monitoring mass transfer in nanoporous materials dates back to late 1970s when Caro and colleagues reported results of investigations of water uptake by LTA type zeolites. It was, however, not before the beginning of the new millennium that the developments in both the measuring technique and computational power have enabled the recording of transient guest profiles during molecular uptake and release under well‐defined conditions, leading to the establishment of a novel access to diffusion studies, now referred to as micro‐imaging. In the present contribution, the thus accessible novel type of information is illustrated by an in‐depth analysis of the uptake kinetics of methanol in an all‐silica ferrierite. In particular, two remarkable experimental findings are reported, which may be tracked back to their microstructural and/or microdynamic origin, namely a pronounced asymmetry in the transient concentration profiles and a slowing down of guest uptake with increasing temperature.     

Large-Scale Hydrogen Production

There is a growing need for hydrogen in processing heavier and dirtier fossil fuels and a future hydrogen economy is widely suggested as the next generation fuel/energy source once fossil fuels diminish in availability. Sustainable fuels are still regarded as too expensive given the large amounts of natural gas and a projected, ample supply of fossil fuels beyond the next twenty-plus years. Today, the steam reforming of hydrocarbons is the most favorable route to H₂. If CO₂ sequestration were ever to become widely practiced, fossil fuels would continue to play an important role in the future hydrogen economy.     

Synthesis of end-branched poly(ethylene glycol)s by aqueous atom transfer radical polymerization

Summary This article reports the synthesis of novel hydrophilic end-branched poly(ethylene glycol)s, in aqueous media by atom transfer radical polymerization (ATRP). Poly(ethylene glycol)s with molecular weights 10,000 and 16,000 were end-functionalized and used as bifunctional initiators for the polymerization of a poly(ethylene glycol) macromonomer with a molecular weight of 2,000 (PEGMA), either by aqueous ATRP or in a watedmethanol (l/l V/V) mixture. For both macroinitiators a DP of 10 was the target, giving an average of 5 branches in each end. The rates of polymerization were of the same order of magnitude when the polymerizations were initiated by either of the two macroinitiators in watedmethanol (l/l V/V). When a bifunctional oligo(ethy1ene glycol) initiator (M_n = 600) was used to study the polymerization of PEGMA in water/methanol a reduction in the rate of polymerization was observed indicating an influence of the molecular weight of the initiator on the rate of polymerization. Received 25 Maich 2002/Revised 8 November 2002/Accepted 8 November 2002 Correspondence to Jorgen Kops     

Conversion of Ethene to Propene by a Dual Function NiSO4/Re2O7/γ-Al2O3 Catalyst

A NiSO₄/Re₂O₇/γ-Al₂O₃ catalyst was prepared by co-impregnation using an aqueous solution of NiSO₄ and [NH₄][ReO₄], which catalyzes direct conversion of ethene to propene at mild reaction condition (323 K, 1 atm). Catalyst deactivation may be caused by coke formation. The two catalytic components appear to work independently of each other.