A functionalized cyclotriphosphazene with four pyrazolyl substituents, N 3 P 3 (MeNC 2 H 4 O)(dmp) 4 where dmp = 3,5-dimethylpyrazole, has been synthesized and characterized. The reaction of this potentially multi-site coordinating cyclotriphosphazene with diorganotin(IV) dichlorides, SnR 2 Cl 2 (R = Ph, Me), leads to dinuclear [(SnPh 2 Cl 2 ) 2 {N 3 P 3 (MeNC 2 H 4 O)(dmp) 4 }] (1) and mononuclear [(SnMe 2 Cl 2 ){N 3 P 3 (MeNC 2 H 4 O)(dmp) 4 }] (2) complexes. These new compounds were characterized by elemental analysis and IR, 1 H, 31 P and 119 Sn NMR spectroscopy. On the basis of these data, in the complex 1 pyrazolylcyclotriphosphazene acts as a bis-bidentate ligand and coordinates to two SnPh 2 Cl 2 molecules via two geminal pyrazolyl nitrogen atoms. As for complex 2, coordination to one SnMe 2 Cl 2 molecule occurs through two nongeminally substituted pyrazolyl nitrogens. The 119 Sn NMR data are consistent with the increasing of coordination number of tin(IV) in solution.