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We present the computational methodology which for the first time allows rigorous twelve-dimensional (12D) quantum calculations of the coupled intramolecular and intermolecular vibrational states of hydrogen-bonded trimers of flexible diatomic molecules. Its starting point is the approach that we introduced recently for fully coupled 9D quantum calculations of the intermolecular vibrational states of noncovalently bound trimers comprised of diatomics treated as rigid. In this paper it is extended to include the intramolecular stretching coordinates of the three diatomic monomers. The cornerstone of our 12D methodology is the partitioning of the full vibrational Hamiltonian of the trimer into two reduced-dimension Hamiltonians, one in 9D for the intermolecular degrees of freedom (DOFs) and another in 3D for the intramolecular vibrations of the trimer, and a remainder term. These two Hamiltonians are diagonalized separately and a fraction of their respective 9D and 3D eigenstates is included in the 12D product contracted basis for both the intra- and intermolecular DOFs, in which the matrix of the full 12D vibrational Hamiltonian of the trimer is diagonalized. This methodology is implemented in the 12D quantum calculations of the coupled intra- and intermolecular vibrational states of the hydrogen-bonded HF trimer on an {\it ab initio} calculated potential energy surface (PES). They reveal several interesting manifestations of significant coupling between the intra- and intermolecular vibrational modes of (HF)$_3$. The 12D calculations also show that the frequencies of the $v=1,2$ HF stretching states of HF trimer are strongly redshifted in comparison to those of the isolated HF monomer. The agreement between the 12D results and the limited spectroscopic data for HF trimer, while satisfactory, leaves room for improvement and points to the need for a more accurate PES.

In this paper we describe the results of picosecond fluorescence polarization (sub-Doppler) experiments designed to determine the role of purely rotational coherence in two jet-cooled molecules: trans-stilbene and anthracene. Observations of the manifestations of purely rotational coherence in t-stilbene are reported. The relationship of purely rotational coherence to molecular parameters (excited state rotational constants and transition dipole directions) is confirmed by comparison of our measurements with the results of the theory described in paper I [P. M. Felker and A. H. Zewail, J. Chem. Phys. 86, 2460 (1987)]. The sum of rotational constants B[script '] and C[script '] of the t-stilbene S1 electronic state is determined with a precision of better than 1 part in 700 (B[script ']+C[script ']=0.5132±0.0007 GHz). The influence of molecular beam expansion conditions and fluorescence detection conditions on our measurements is also investigated and compared with the theroretical findings of paper I. Also measurements of time-resolved and polarization-analyzed fluorescence as a function of excess vibrational energy in the S1 electronic states of both t-stilbene and anthracene are reported. We are able to distinguish the contribution of purely rotational coherence from the contributions of purely vibrational (or rovibrational) coherence to the evolution of fluorescence from the vibrationally excited molecule. The results are first analyzed on the basis of a model in which strict separability of vibrational and rotational motion is assumed. This provides a test of the extent of coupling of these motions and its influence on intramolecular vibrational energy redistribution (IVR).