Nickela‐electrocatalyzed Mild C−H Alkylations at Room Temperature

Direct alkylations of carboxylic acid derivatives are challenging and particularly nickel catalysis commonly requires high reaction temperatures and strong bases, translating into limited substrate scope. Herein, nickel‐catalyzed C?H alkylations of unactivated 8‐aminoquinoline amides have been realized under exceedingly mild conditions, namely at room temperature, with a mild base and a user‐friendly electrochemical setup. This electrocatalyzed C?H alkylation displays high functional group tolerance and is applicable to both the primary and secondary alkylation. Based on detailed mechanistic studies, a nickel(II/III/I) catalytic manifold has been proposed.     

Ruthenium(II)‐Catalyzed C?H Alkenylations of Phenols with Removable Directing Groups

Cationic ruthenium(II) complexes enabled oxidative alkenylations of phenols bearing easily cleavable directing groups. The optimized catalytic system allowed twofold C? H bond activations with excellent chemo‐, site‐, and diastereoselectivities. The double C? H functionalization process proceeded efficiently in an aerobic fashion under an atmosphere of ambient air. Detailed mechanistic studies were performed and provided strong support for an initial reversible C? H bond activation by the formation of six‐membered ruthenacycles as the key intermediates.     

Study of multi-nucleon transfer reactions in 58, 64Ni + 207Pb collisions at the velocity filter SHIP

The European Physical Journal A - We investigated multi-nucleon transfer reactions in collisions of 58Ni + 207Pb and 64Ni + 207Pb at Coulomb barrier energies. The new aspect is that we used a...     

Selective oxidation of cyclooctane to cyclootanone with molecular oxygen in the presence of compressed carbon dioxide

The oxidation of cyclooctane (1) to cyclooctanone (3) with molecular oxygen and acetaldehyde (2) as a co-reductant occurs efficiently in the presence of compressed CO2. Up to 20% yields of 3 are obtained under optimised multiphase conditions.     

Self-diffusion rates in Al from combined first-principles and model-potential calculations

Monovacancy diffusion alone dominates over diffusion due to divacancies and interstitials in Al for all temperatures up to the melting point. Deviations from a single Arrhenius dependence are due to anharmonicity. The conclusion is based on a combination of theoretical methods, from density functional theory to thermodynamic integration, without fitting to experimental data. The calculated diffusion rate agrees with experimental data over 11 orders of magnitude.     

Taking a strategic view of BPR to develop a multidisciplinary framework

Despite undoubtedly being one of the latest fads, Business Process Reengineering (BPR) has provoked much debate about how organisations should be managed if dramatic improvements in performance are to be achieved. This paper takes a multidisciplinary view of BPR and focuses upon a number of the emergent issues. These include the role of strategy making, the promotion of communication and creativity, the role of statistics, and the effective use of performance measurement systems within a learning environment. The paper develops a framework that capitalises on the role of modelling in MS/OR as well as the various disciplines of the authors. As such, the framework draws on recent advances, as well as established thinking, in the areas of strategy development, information systems, quality management and statistical science. More importantly, the framework also provides an iterative approach to BPR enabling organisations to design, implement and monitor progress on an ongoing basis. Emphasis is placed on building effective communications, developing an organisational memory and supporting organisational learning.     

Untersuchungen zur anwendung ternärer komplexe in der photometrie—III: Die bestimmung des titanium(iv) mit brompyrogallolrot in gegenwart von nitrilotriessigsäure bzw. ethylenediamintetraessigsäure

As part of a continued investigation of the analytical applications of ternary complexes, the systems Ti(IV)/BPR, I), Ti(IV)/BPR/EDTA (II), and Ti(IV)/BPR/NTA (III), where BPR = Bromopyrogallol Red, have been investigated and compared in terms of working concentration range, molar absorptivity, standard deviation, coefficient of variation, calibration sensitivity, limit of detection and of determination. A novel way of summarizing the effects of interferences of a large group of ions (some 47 in all) is presented. The results show that the ternary systems, in particular system II, have a better selectivity than the simple binary system I of titanium with Bromopyrogallol Red.