Two previously reported 1, 3,5,7,3,6, chloride platinum(II) complexes [PtCl{HN=C(R)N=CN[C(Ph)=C(Ph)]C=NC(R)=NH}] (R = t Bu 1, Ph 2) form solvates with halomethanes 1•1¼CH2Cl2, 1•1⅖CH2Br2, and 2•CHCl3. All these species featuring novel complex-solvent heterotetrameric clusters, where the structural units are linked by simultaneous two C-X•••Cl-Pt (X = Cl, Br) halogen and two C-H•••Cl-Pt hydrogen bonds. The geometric parameters of these weak interactions were determined by single-crystal XRD, and the nature of XB's and HB's in the clusters were studied for the isolated model systems (1)2•(CH2Cl2)2, (1)2•(CH2Br2)2, and (2)2•(CHCl3)2 by DFT calculations and Bader's AIM analysis. The evaluated energies of the weak interactions are in the range 0.9-3.0 kcal/mol. The XB's and HB's in the reported clusters are cooperative. In the cases of (1)2•(CH2Cl2)2 and (1)2•(CH2Br2)2, the contribution of HB's to the stabilization of the system is dominant, whereas for (2)2•(CHCl3)2 contributions of both types of non-covalent interactions are almost the same. Crystal packing and other forces such as, e.g. dipole-dipole interactions, also affect the formation of the clusters.