Vibrational molecular quantum computing: basis set independence and theoretical realization of the Deutsch-Jozsa algorithm

The phase of quantum gates is one key issue for the implementation of quantum algorithms. In this paper we first investigate the phase evolution of global molecular quantum gates, which are realized by optimally shaped femtosecond laser pulses. The specific laser fields are calculated using the multitarget optimal control algorithm, our modification of the optimal control theory relevant for application in quantum computing. As qubit system we use vibrational modes of polyatomic molecules, here the two IR-active modes of acetylene. Exemplarily, we present our results for a Pi gate, which shows a strong dependence on the phase, leading to a significant decrease in quantum yield. To correct for this unwanted behavior we include pressure on the quantum phase in our multitarget approach. In addition the accuracy of these phase corrected global quantum gates is enhanced. Furthermore we could show that in our molecular approach phase corrected quantum gates and basis set independence are directly linked. Basis set independence is also another property highly required for the performance of quantum algorithms. By realizing the Deutsch-Jozsa algorithm in our two qubit molecular model system, we demonstrate the good performance of our phase corrected and basis set independent quantum gates.     

Evolution of Oxygen–Metal Electron Transfer and Metal Electronic States During Manganese Oxide Catalyzed Water Oxidation Revealed with In Situ Soft X‐Ray Spectroscopy

Manganese oxide (MnO_x) electrocatalysts are examined herein by in situ soft X‐ray absorption spectroscopy (XAS) and resonant inelastic X‐ray scattering (RIXS) during the oxidation of water buffered by borate (pH 9.2) at potentials from 0.75 to 2.25 V vs. the reversible hydrogen electrode. Correlation of L‐edge XAS data with previous mechanistic studies indicates Mn^IV is the highest oxidation state involved in the catalytic mechanism. MnO_x is transformed into birnessite at 1.45 V and does not undergo further structural phase changes. At potentials beyond this transformation, RIXS spectra show progressive enhancement of charge transfer transitions from oxygen to manganese. Theoretical analysis of these data indicates increased hybridization of the Mn?O orbitals and withdrawal of electron density from the O ligand shell. In situ XAS experiments at the O K‐edge provide complementary evidence for such a transition. This step is crucial for the formation of O₂ from water.     

Selective N,O‐Addition of the TEMPO Radical to Conjugated Boryldienes

B(C₆F₅)₂‐containing boryldienes 4 underwent the addition of two molar equivalents of TEMPO to give N,O‐bonded four‐membered heterocyclic products 7 . The reaction is a metal‐free example of the generation of reactive nitrogen‐centered TEMPO radical derivatives, in this case by the addition of TEMPO to the borane, followed by carbon–nitrogen bond formation and subsequent trapping of the resulting allyl radical by the second equivalent of TEMPO.     

Reduced formation of peroxide and radical species stabilises iron-based hybrid catalysts in polymer electrolyte membrane fuel cells

The incorporation of Pt into an iron-nitrogen-carbon(Fe NC)catalyst for the oxygen reduction reaction(ORR)was recently shown to enhance catalyst stability without Pt directly contributing to the ORR activity.However,the mechanistic origin of this stabilisation remained obscure.It is established herein with rotating ring disc experiments that the side product,H₂O₂,which is known to damage FeNC catalysts,is suppressed by the presence of Pt.The formation of reactive oxygen species is additionally inhibited,independent of intrinsic H₂O₂ formation,as determined by electron paramagnetic resonance.Transmission electron microscopy identifies an oxidised Fe-rich layer covering the Pt particles,thus explaining the inactivity of the latter towards the ORR.These insights develop understanding of Fe NC degradation mechanisms during ORR catalysis,and crucially establish the required properties of a precious metal free protective catalyst to improve Fe NC stability in acidic media.     

Aminocarbonylthioformiate – Darstellung und Reaktionen

Aminocarbonylthioformates — Preparation and Reactivity Sodium aminocarbonylthioformate NaSCOCONH₂ (II) is obtained by reaction of sodium cyanodithioformate with acetone in presence of a secondary amine and water. II permits to produce the acid HSCOCONH₂ · H₂O (IX) and salts M^II(SCOCONH₂)₂ · 2H₂O. In basic aqueous solutions hydrolysis of II to oxaminate and oxalate, respectively, takes place, an excess of aqueous ammonia leads to amidino formic acid. In organic solvents the reaction of IX with N-bases yields stable ammonium salts. The results of i.r. spectroscopic and thermogravimetric measurements are discussed.     

Coal analysis by application of the partial least squares method to infrared spectra

Summary A method for the rapid characterization of brown coals based on the application of a powerful method of principal component analysis, the Partial Least Squares method (PLS), is described. A data catalogue of 44 brown coals from different deposits of East European and Asian countries was used, which lists analyses of several coal parameters. Infrared spectra of brown coals were recorded and different coal properties were predicted with the help of PLS. The results show that, with the PLS-method used, several coal properties can be predicted and it is possible to describe the classification of a coal for several technological processes. The developed method is useful because of the multiplicity of information obtained within a short time and because it is possible to replace lengthy classical methods.     

Proton and triton momentum distributions from4He fragmentation at relativistic energies

The 0° differential cross sections of the¹²C(⁴He,p) and¹²C(⁴He,t) reactions have been measured at beam momenta of 4.52 and 2.69 GeV/c/nucleon, respectively. The proton and triton momentum distributions in⁴He are extracted from the cross sections using a relativistic impulse approximation. Some theoretical models based on realisticN-N potentials are examined for our data.