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A new framework for $A(d,p)B$ reactions is introduced by merging the microscopic approach to computing the properties of the nucleon-target systems and the three-body $n+p+A$ reaction formalism, thus providing a consistent link between the reaction cross sections and the underlying microscopic structure. In this first step toward a full microscopic description, we focus on the inclusion of the neutron-target microscopic properties. The properties of the neutron-target subsystem are encapsulated in the Greens function which is computed with the Coupled Cluster theory using a chiral nucleon-nucleon and three-nucleon interactions. Subsequently, this many-body information is introduced in the few-body Greens Function Transfer approach to $(d,p)$ reactions. Our benchmarks on stable targets $^{40,48}$Ca show an excellent agreement with the data. We then proceed to make specific predictions for $(d,p)$ on neutron rich $^{52,54}$Ca isotopes. These predictions are directly relevant to testing the new magic numbers $N=32,34$ and are expected to be feasible in the first campaign of the projected FRIB facility.
A current interest in nuclear reactions, specifically with rare isotopes concentrates on their reaction with neutrons, in particular neutron capture. In order to facilitate reactions with neutrons one must use indirect methods using deuterons as beam
The finite range adiabatic wave approximation provides a practical method to analyze (d,p) or (p,d) reactions, however until now the level of accuracy obtained in the description of the reaction dynamics has not been determined. In this work, we perf
The description of nuclei starting from the constituent nucleons and the realistic interactions among them has been a long-standing goal in nuclear physics. In addition to the complex nature of the nuclear forces, with two-, three- and possibly highe
A method to calculate reactions in quantum mechanics is outlined. It is advantageous, in particular, in problems with many open channels of various nature i.e. when energy is not low. In the method there is no need to specify reaction channels in a d
The method of integral transforms is reviewed. In the framework of this method reaction observables are obtained with the bound--state calculation techniques. New developments are reported.