Constrained optimization refers to the optimization of molecular structures in
which certain parameters (e.g., bond lengths, bond angles or dihedral angles)
are fixed. In quantum chemistry calculations, this has traditionally been
accomplished using Z-matrix coordinates, with the desired parameter set in
the Z-matrix and simply omitted from the optimization space. In 1992, Baker
presented an algorithm for constrained optimization directly in Cartesian
J. Comput. Chem.
(1992), 13, pp. 240. Baker’s algorithm used both penalty functions and the classical method of Lagrange multipliers, and was developed in order to impose constraints on a molecule obtained from a graphical model builder as a set of Cartesian coordinates. Some improvements widening the range of constraints that could be handled were made in 1993. 49 J. Comput. Chem.
(1993), 14, pp. 1339. Q-Chem includes the latest version of this algorithm, which has been modified to handle constraints directly in delocalized internal coordinates. 54 J. Comput. Chem.
(1997), 18, pp. 1079.
The essential problem in constrained optimization is to minimize a function of, for example, variables subject to a series of m constraints of the form fpr . Assuming , then perhaps the best way to proceed (if this were possible in practice) would be to use the constraint equations to eliminate of the variables, and then solve the resulting unconstrained problem in terms of the independent variables. This is exactly what occurs in a Z-matrix optimization. Such an approach cannot be used in Cartesian coordinates as standard distance and angle constraints are non-linear functions of the appropriate coordinates. For example a distance constraint (between atoms and in a molecule) is given in Cartesians by , with
and the constrained distance. This obviously cannot be satisfied by elimination. What can be eliminated in Cartesians are the individual , and coordinates themselves and in this way individual atoms can be totally or partially frozen.
Internal constraints can be handled in Cartesian coordinates by introducing the Lagrangian function
which replaces the function in the unconstrained case. Here, the are the so-called Lagrange multipliers, one for each constraint . Differentiating Eq. (A.18) with respect to and affords
At a stationary point of the Lagrangian we have , i.e., all and all . This latter condition means that all and thus all constraints are satisfied. Hence, finding a set of values (, ) for which will give a possible solution to the constrained optimization problem in exactly the same way as finding an for which gives a solution to the corresponding unconstrained problem.
The Lagrangian second derivative matrix, which is the analogue of the Hessian matrix in an unconstrained optimization, is given by
Thus, in addition to the standard gradient vector and Hessian matrix for the
unconstrained function , we need both the first and second
derivatives (with respect to coordinate displacement) of the constraint
functions. Once these quantities are available, the corresponding Lagrangian
gradient, given by Eq. (A.19), and Lagrangian second derivative matrix, given by
Eq. (A.21), can be formed, and the optimization step calculated in a similar
manner to that for a standard unconstrained optimization.
J. Comput. Chem.
(1992), 13, pp. 240.
In the Lagrange multiplier method, the unknown multipliers, , are an integral part of the parameter set. This means that the optimization space consists of all variables plus all Lagrange multipliers , one for each constraint. The total dimension of the constrained optimization problem, , has thus increased by compared to the corresponding unconstrained case. The Lagrangian Hessian matrix, , has extra modes compared to the standard (unconstrained) Hessian matrix, . What normally happens is that these additional modes are dominated by the constraints (i.e., their largest components correspond to the constraint Lagrange multipliers) and they have negative curvature (a negative Hessian eigenvalue). This is perhaps not surprising when one realizes that any motion in the parameter space that breaks the constraints is likely to lower the energy.
Compared to a standard unconstrained minimization, where a stationary point is
sought at which the Hessian matrix has all positive eigenvalues, in the
constrained problem we are looking for a stationary point of the Lagrangian
function at which the Lagrangian Hessian matrix has as many negative
eigenvalues as there are constraints (i.e., we are looking for an th-order
saddle point). For further details and practical applications of
constrained optimization using Lagrange multipliers in Cartesian coordinates;
J. Comput. Chem.
(1992), 13, pp. 240. .
Eigenvector following can be implemented in a constrained optimization in a similar way to the unconstrained case. Considering a constrained minimization with constraints, then Eq. (A.11) is replaced by
and Eq. (A.12) by
where now the are the eigenvalues of , with corresponding eigenvectors , and . Here Eq. (A.25) includes the constraint modes along which a negative Lagrangian Hessian eigenvalue is required, and Eq. (A.26) includes all the other modes.
Equations (A.25) and (A.26) implement eigenvector following for a constrained minimization. Constrained transition state searches can be carried out by selecting one extra mode to be maximized in addition to the constraint modes, i.e., by searching for a saddle point of the Lagrangian function of order .
It should be realized that, in the Lagrange multiplier method, the desired constraints are only satisfied at convergence, and not necessarily at intermediate geometries. The Lagrange multipliers are part of the optimization space; they vary just as any other geometrical parameter and, consequently the degree to which the constraints are satisfied changes from cycle to cycle, approaching 100% satisfied near convergence. One advantage this brings is that, unlike in a standard Z-matrix approach, constraints do not have to be satisfied in the starting geometry.
Imposed constraints can normally be satisfied to very high accuracy,
or better. However, problems can arise for both bond and dihedral angle
constraints near and and, instead of attempting to
impose a single constraint, it is better to split angle constraints near these
limiting values into two by using a dummy atom,
J. Comput. Chem.
(1993), 14, pp. 1339. exactly analogous to splitting a bond angle into two angles in a Z-matrix.
Note: Exact and single angle constraints cannot be imposed, as the corresponding constraint normals, , are zero, and would result in rows and columns of zeros in the Lagrangian Hessian matrix.