The new planar tetracoordinate carbon (ptC) compounds have received significant research attention in recent years. The present study is devoted to investigating the structural, electronic, and magnetic features of one-dimensional chains and two-dimensional sheets composed of C2Al14(CH3)(8) building blocks. All possible condensations were studied, and the stabilities of different ptC assemblies were compared. Several properties such as energy gap, dipole polarizability, electronic excitation energies, and nucleus chemical shift were computed for chains up to 7 and sheets up to 16 units. A systematic analysis was performed to assess the impact of condensation pattern and number of units on the calculated properties. Topological analysis of density and electron localization functions reveals that Al-C bonds in the considered ptCs have mixed covalent/ionic character with larger ionic contribution. It is found that the electronic spectra of the condensed ptCs exhibit red shift toward larger wavelengths when compared to the C2Al14(CH3)(8) building block. The amount of red shift enhances with increasing number of units. We show that the stability trend, predicted by electronic and magnetic descriptors, are in qualitative agreement with the thermodynamic stability obtained through Gibbs free energy change of condensation reaction.