Chemical reaction dynamics studies emerged with the advent of quantum mechanical theories in 1920s which have the capability of predicting the atomic motions by calculating potential energy surfaces. Experimental studies in this field began to flourish with the advances in molecular beam generation and laser beam technologies many years later leading to the Nobel prize awarded to Herschbach, Lee, and Polanyi in 1986. Later in 1980s, advances in the production of frequency tunable ultrashort laser pulses with the temporal resolution of femtoseconds led to the birth of the field of femto-chemistry which is the study of molecular dynamics in real time. In the last few decades, various spectroscopic techniques exploiting ultrashort laser pulses have been developed to study the non-adiabatic dynamics of molecules in real time and space. Laser-induced Coulomb Explosion Imaging (CEI) is a powerful probe technique now emerging in this field, to unravel the structural changes of molecular systems in real time. Extracting structural information from CEI requires imaging of multiple fragments at each experimental cycle which allows us to obtain their relative velocity distribution. In this work, we successfully coupled a three-dimensional multi-mass coincidence detection technique with CEI to study the dissociation dynamics of complicated polyatomic molecules. Covariance imaging, which is a statistical technique yielding correlated information, was used to find the related momenta of various pairs of ions and reveal different dissociation channels of the parent multi-cation. Using the combination of these techniques, the strong field dissociative ionization of chlorocarbonylsulfenyl chloride (CCSC) and methoxycarbonylsulfenyl chloride (MCSC) (belonging to thioester family) were studied. The ultrafast electron diffraction (UED) technique is a complementary method to ultrafast laser spectroscopy, capable of directly resolving the electronic and nuclear dynamics in real time and space due to sensitivity to the spatial atomic distribution in the system. MeV UED facility is a newly developed apparatus at the SLAC National Accelerator Laboratory offering femtosecond time resolution and sub-Angstrom spatial resolution in the study of gas phase molecular systems. Using this facility, we performed a time-resolved UED experiment to study the UV photodissociation of oxalyl chloride. Previous theoretical and experimental studies have suggested non-consistent results for the UV dissociation of this molecule which results in four fragments upon absorption a single photon. Here, with the initial analysis of diffraction images, and comparison with the theory, we confirmed a concerted four-body dissociation channel as the main mechanism.