ABSTRACT:A new zeolite (named as ITQ-52) having large cavities and small and medium channels has been synthesized. This was achieved by using a new family of aminophosphonium cations as organic structure directing agent (OSDA). These cations contain P-C and P-N bonds, and therefore they lie between previously reported P-containing OSDA, such as tetraalkylphosphonium and phosphazenes. In this study, it has been found that 1,4-butane-diylbis[tris(dimethylamino)]phosphonium dication is a very efficient OSDA for crystallization of several zeolites, and in some particular conditions, the new zeolite ITQ-52 was synthesized as a pure phase. The structure of ITQ-52 has been solved using high resolution synchrotron X-Ray powder diffraction data of the calcined solid. This new zeolite crystallizes in the space group I2/m, with cell parameters a = 17.511 Å, b = 17.907 Å, c = 12.367 Å and β = 90.22 º. The topology of ITQ-52 can be described as a replication of a Composite Building Unit with ring notation [4 3 5 4 6 1 ] that gives rise to the formation of an interconnected 8R and 10R-channel system. Typically, zeolites can be described as crystalline silicabased microporous solids that can carry out a myriad of different processes when doped with the appropriated active sites, such as Al, B, Ga, Ge, Ti, Sn, etc. The catalytic performance of the final porous solids depends mainly on the nature of the heteroatom as well as on their structural pore topologies. Zeolites have been applied for gas adsorption, separation, catalysis, encapsulation or controlled release of molecules, among others, some of them are of industrial application. [1][2][3][4][5][6][7][8][9] There is no doubt that this is the driving force for synthesizing new zeolite structures.Most of the zeolites described in the literature have been obtained by employing tetraalkylammonium cations as organic structure directing agents (OSDAs). 10-13 Recently, we have reported a number of new zeolites synthesized by using tetraalkylphosphonium cations 14 15 and ITQ-49 17 ) or phosphazenes (ITQ-47 18 ) as OSDAs. The success of using phosphorous-containing cations as OSDA for zeolite crystallization has moved us to look for different alternatives of organophosphorous cations that are easy and safe to prepare. Then, we found in literature that Wittig-like cations can be quantitatively prepared from the commercially available aminophosphines resulting in phosphorous containing cations. [19][20][21][22] These new organocations are related to phosphazenes and tetraalkylphosphonium, since they contain P-N and P-C bonds (see fig. S1 in Supporting Information). On those bases, we have developed a new family of amino-phosphonium cations that introduce interesting features from the point of view of OSDAs for zeolite synthesis. Then, the amino-phosphonium cationic compounds have been used for zeolite synthesis, and here we describe the synthesis and crystal structure of a new zeolite, named as ITQ-52, that was obtained by using 1,4-butane-diylbis[tris(dimethylamino)]phosphonium di...