Takeshi Yanai 교수

We propose a theory to describe dynamic correlations in bonding situations where there is also significant nondynamic character. We call this the canonical transformation (CT) theory. When combined with a suitable description of nondynamic correlation, such as given by a complete-active-space self-consistent Field (CASSCF) or density matrix renormalization group wave function, it provides a theory to describe bonding situations across the entire potential energy surface with quantitative accurac

The recent advent of the density matrix renormalization group (DMRG) theory has delivered a new capability to compute multireference (MR) wave function with large configuration space, which far exceeds the limitation of conventional approaches. Here, we provide an overview of our recent work on the developments of ab initio DMRG methods in the context of the active space approaches and their applications to MR chemical systems. © 2014 Wiley Periodicals, Inc.

We describe the joint application of the density matrix renormalization group and canonical transformation theory to multireference quantum chemistry. The density matrix renormalization group provides the ability to describe static correlation in large active spaces, while the canonical transformation theory provides a high-order description of the dynamic correlation effects. We demonstrate the joint theory in two benchmark systems designed to test the dynamic and static correlation capabilitie

The canonical transformation theory of Yanai and Chan [J. Chem. Phys. 124, 194106 (2006)] provides a rigorously size-extensive description of dynamical correlation in multireference problems. Here we describe a new formulation of the theory based on the extended normal ordering procedure of Mukherjee and Kutzelnigg [J. Chem. Phys. 107, 432 (1997)]. On studies of the water, nitrogen, and iron oxide potential energy curves, the linearized canonical transformation singles and doubles theory is comp

A multiresolution solver for fully numerical linear response calculations of excitation states via the time-dependent Hartree–Fock and density functional theory (TD-HF/DFT) is presented. The linear response method Yanai et al. previously reported [J. Chem. Phys., submitted] was limited to the Tamm–Dancoff approximation and could only use the Hartree–Fock exchange and the local-spin density approximation (LSDA) with a crude asymptotic correction. The present development enables us to perform full

Abstract An algorithm that accelerates the convergence of the iterative optimization of the complete active space self‐consistent field (CASSCF) wavefunction so as to find a optimum solution in fewer macroiterations is described. The algorithm is oriented to large‐scale CASSCF problems that are to be solved with a combination of density matrix renormalization group (DMRG) method for the configuration interaction (CI) process. The algorithm is based on the alternating (or two‐step) CASSCF optimiz

In a previous study we reported an efficient, accurate multiresolution solver for the Kohn-Sham self-consisitent field (KS-SCF) method for general polyatomic molecules. This study presents an efficient numerical algorithm to evalute Hartree-Fock (HF) exchange in the multiresolution SCF method to solve the HF equations. The algorithm employs fast integral convolution with the Poission kernel in the nonstandard form, screening the sparse multiwavelet representation to compute results of the integr

A highly efficient computational scheme for four-component relativistic ab initio molecular orbital (MO) calculations over generally contracted spherical harmonic Gaussian-type spinors (GTSs) is presented. Benchmark calculations for the ground states of the group IB hydrides, MH, and dimers, M2 (M=Cu, Ag, and Au), by the Dirac–Hartree–Fock (DHF) method were performed with a new four-component relativistic ab initio MO program package oriented toward contracted GTSs. The relativistic electron rep

An efficient and accurate analytic gradient method is presented for Hartree-Fock and density functional calculations using multiresolution analysis in multiwavelet bases. The derivative is efficiently computed as an inner product between compressed forms of the density and the differentiated nuclear potential through the Hellmann-Feynman theorem. A smoothed nuclear potential is directly differentiated, and the smoothing parameter required for a given accuracy is empirically determined from calcu

An effective Hamiltonian perturbed with explicit interelectronic correlation is derived from similarity transformation of Hamiltonian using a unitary operator with Slater-type geminals. The Slater-type geminal is projected onto the excitation (and deexcitation) component as in the F12 theory. Simplification is made by truncating higher-body operators, resulting in a correlated Hamiltonian which is Hermitian and has exactly the same complexity as the original Hamiltonian in the second quantized f

A new four-component Dirac–Kohn–Sham (DKS) method is presented. The method provides a computationally efficient way to perform fully relativistic and correlated ground state calculations on heavy-atom molecular systems with reliable accuracy. The DKS routine has been implemented in the four-component Dirac–Hartree–Fock program system REL4D. Two-component generally contracted, kinetically balanced Gaussian-type spinors (GTSs) are used as basis spinors. The one-electron and Coulomb integrals are c

Abstract We report on the fluorescence properties of a new class of emissive and stable π‐radicals that contain a boron atom at a position distant from the radical center. A fully planarized derivative exhibited an intense red fluorescence with high fluorescence quantum yields ( Φ F >0.67) even in polar solvents. To elucidate the origin of this phenomenon, we synthesized another boron‐stabilized radical that contains a bulky aryl group on the boron atom. A comparison of these derivatives, as

We present the development of the multistate multireference second-order perturbation theory (CASPT2) with multiroot references, which are described using the density matrix renormalization group (DMRG) method to handle a large active space. The multistate first-order wave functions are expanded into the internally contracted (IC) basis of the single-state single-reference (SS-SR) scheme, which is shown to be the most feasible variant to use DMRG references. The feasibility of the SS-SR scheme c

Theoretical study has been given on bifurcating reaction paths where the intrinsic reaction path (IRP) has a valley-ridge inflection (VRI) point on the way from transition state to product, and leads to another first-order saddle point which connects two symmetrically equivalent products. To extract dynamically important regions in the configuration space between the VRI point and products, a group of steepest descent paths are calculated starting from zero-point energy regions at the VRI point,