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In the first step of the approach, a number of quantum mechanical calculations are performed to predict the relative rate constant for the reaction of interest in several solvents.
Also quantitative structure activity relationship approach has been used to establish the correlations between a number of quantum chemical parameters and the molecular structures of some gum extracts major components.
This is well justified for Rydberg blockade quantum computing with optical excitation of neutral atoms, but it also applies for a number of quantum computing proposals with similarly isolated and identifiable qubits.
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A proposal for a number of interesting quantum algorithms is presented, in the frame of the coupled quantum-wires physical system.
A cell in the mQCA model consists of a number of molecular quantum dots (or redox centers) and a few electrons.
One of the great advantages of the FMO method is that it can be combined with a number of current quantum chemical techniques.
Rigetti also today announced that it is partnering with a number of leading quantum computing startups (the kind that work on the software, not the hardware side of this ecosystem).
Craddock et al. (2015) point out a number of possible quantum effects (including the power-law behavior addressed by Vitiello, cf. Section 4.3) which can be investigated using presently available technologies.
In the last two decades, a number of semiconductor quantum and nanostructures (QNSs) by the strain-driven self-assembly based on Stranski-Krastanow (S-K) growth[1] have been demonstrated in the field of epitaxial growth using molecular beam epitaxy (MBE).
However, as argued by Bueno (Bueno 2003), Balaguer's strategy is incompatible with a number of interpretations of quantum mechanics, in particular with Bas van Fraassen's version of the modal interpretation (van Fraassen 1991).
The propagation of a wave packet composed of fixed-width Gaussian functions allows a one-to-one mapping between the quantum dynamics results and a small number of quantum trajectories, allowing electronic structure theory calculations to be performed preferentially in dynamically-important regions.
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Justyna Jupowicz-Kozak
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