The possibility of exploiting a thermally-induced solid-state reaction to obtain the formation of a fluorene and TCNQ molecular complex was proposed by some of us (Kumar et al. Crystal Growth & Design, 2009, 9(8), 3396-3404). In this paper, we generalize and rationalize the approach to other charge transfer (CT) molecular complexes with naphthalene and anthracene, changing the size of the donor moiety to propose a general approach for the preparation of this class of materials by exploiting the solid-state synthesis method. Moreover, the kinetic features of the solid state reactions were fully elucidated by Raman spectroscopy and High Resolution X-ray Powder Diffraction analysis (in situ Raman/XRPD), exploiting the Avrami equation in isothermal and non-isothermal conditions, rate constants, reaction orders and activation energies were obtained. All the three tested solid-state charge transfer (SS-CT) reactions resulted to obey a general rule, whereby predicting the most apt reaction temperature. Finally, a method based on principal component analysis (PCA) for a fast kinetic analysis of in situ XRD synchrotron data was successfully developed, employing a formalism suitable for the analysis of non-isothermal reaction data, thus allowing a high throughput approach for the fast screening of the kinetics of parent reactions. PCA analysis was exploited as an alternative technique to obtain kinetic information in a faster and more efficient way, which can be used for on line monitoring and/or in all those cases where Rietveld analysis is not feasible. Figure 4 Initial (a) and final (b) Raman spectra for NA-TCNQ formation reaction and variation of the Raman peak of TCNQ at 1600 cm -1 within time (c). Reaction coordinates and kinetic analysis (Kennedy and Clark approach) of Raman data for NA-TCNQ (d and e) and FL-TCNQ (f and g). Linear fit of NA-TCNQ (b): Equation y=-8421 (1438)*x+20(4) Rsq. = 0.847. Ea = 70kJ/mol. Linear fit of FL-TCNQ (d): Equation y=-21443 (3562)*x+55(10.) Rsq. = 0.854. Ea = 178kJ/mol