We extend the traditional conceptual density functional theory (CDFT) to conceptual density matrix functional theory (CDMFT) by replacing the external potential v(r) by the one-electron integral hrs in the energy functional. This approach provides a new path for investigating intrinsic bond properties such as bond reactivity. The derivation of the Fukui matrix, i.e., derivative of the density matrix P with respect to the number of electrons N, is elucidated, and the result is illustrated in a case study on H2O. The matrix is shown to play a crucial role in quantifying changes of bond strength for electron removal or addition processes via the bond order derivative . Using the Mayer bond order and different atoms-in-molecules partitioning methods, we show that as a first-order response quantity, the bond order derivative agrees well with the finite difference bond order changes. The bond order derivative (bond Fukui function) is a bond reactivity descriptor. We demonstrate this by predicting the regioselectivity of a classical electrophilic addition reaction (the bromination of alkenes) and predicting the initial electron-driven bond cleavage in mass spectrometry. Specifically, the bond order derivative captures all of the major signals from the experimental mass spectra for a series of small molecules with a variety of functional groups.
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