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The present invention provides compositions of crystalline coordination copolymers wherein multiple organic molecules are assembled to produce porous framework materials with layered or core-shell structures. These materials are synthesized by sequential growth techniques such as the seed growth tec

The present invention provides compositions of crystalline coordination copolymers wherein multiple organic molecules are assembled to produce porous framework materials with layered or core-shell structures. These materials are synthesized by sequential growth techniques such as the seed growth technique. In addition, the invention provides a simple procedure for controlling functionality.

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1. A method of making a coordination copolymer comprising: a) adding at least one source of metal cations and at least one organic linking compound to a solvent to form a first solution or colloidal suspension;b) treating the first solution or colloidal suspension to form crystals of a first coordin

1. A method of making a coordination copolymer comprising: a) adding at least one source of metal cations and at least one organic linking compound to a solvent to form a first solution or colloidal suspension;b) treating the first solution or colloidal suspension to form crystals of a first coordination polymer having a first x-ray diffraction pattern;c) adding at least one source of metal cations and at least one organic linking compound to a solvent to form a second solution or colloidal suspension wherein the second solution is not identical to the first solution or colloidal suspension;d) adding crystals of the first coordination polymer to the second solution or colloidal suspension; ande) treating the second solution or colloidal suspension to form crystals of a second coordination polymer having a second x-ray diffraction pattern as a layer over one or more crystals of the first coordination polymer forming a coordination copolymer comprising at least a first region of the first coordination polymer and at least a second region of a second coordination polymer wherein the first coordination polymer is not identical to the second coordination polymer and wherein the x-ray diffraction pattern of the coordination copolymer comprises both the first x-ray diffraction pattern and the second x-ray diffraction pattern. 2. The method of claim 1 wherein the crystals of the first coordination polymer are of a size ranging from about 10 nanometers to about 1 micron. 3. The method of claim 1 wherein the treating of steps 1b and le comprise temperatures ranging from ambient to about 250° C. and reaction times from about 1 minutes to about 5 months. 4. The method of claim 1 wherein the treating of steps 1 b and 1 e comprise temperatures ranging from ambient to about 125° C. and reaction times from about 2 hours to about 4 days. 5. The method of claim 1 wherein the solvent is selected from the group consisting of formamides, sulfoxides, nitriles, esters, amines, ethers, ketones, aromatics, aliphatics, water, and combinations thereof. 6. The method of claim 1 further comprising: f) adding at least one source of metal cations and at least one organic linking compound to a solvent to form a third solution or colloidal suspension wherein the third solution or colloidal suspension is not identical to the first or second solutions or colloidal suspensions;g) adding the coordination copolymer of 1 e) to the third solution or colloidal suspension; andh) treating the third solution or colloidal suspension to form crystals of a third coordination polymer as a layer over one or more crystals of the coordination copolymer forming a second coordination copolymer wherein the third coordination polymer has a different composition or structure than that of the second coordination polymer. 7. The method of claim 1 further comprising: i) adding at least one source of metal cations and at least one organic linking compound to a solvent to form a third solution or colloidal suspension wherein the third solution or colloidal suspension is identical to the first solution or colloidal suspension;j) adding the coordination copolymer of 1 e) to the third solution or colloidal suspension; andk) treating the third solution or colloidal suspension to form crystals of a third coordination polymer as a layer over one or more crystals of the coordination copolymer forming a second coordination copolymer wherein the third coordination polymer is the same as the first coordination polymer. 8. The method of claim 1 further comprising, selecting at least one organic linking compound in the first solution or colloidal suspension and at least one organic linking compound in the second solution or colloidal suspension to control a characteristic of the coordination copolymer. 9. The method of claim 1 further comprising: l) adding the coordination copolymer of 1 e) to the first solution or colloidal suspension; andm) treating the first solution or colloidal suspension to form crystals of the first coordination polymer as a third layer over one or more crystals of the coordination copolymer forming a second coordination copolymer wherein the third layer has the same composition and structure as that of the first layer. 10. A method of making a coordination copolymer comprising: a) adding at least one source of metal cations and at least one organic linking compound in a solvent to form a solution or colloidal suspension;b) treating the solution or colloidal suspension to form crystals of a first coordination polymer having a first e-ray diffraction pattern;c) adding at least one additional reagent selected from the group consisting of a second source of metal cations, a second organic linking compound, and a combination thereof, to the solution or colloidal suspension; andd) treating the solution to form crystals of a second coordination polymer having a second x-ray diffraction pattern as layer over one or more crystals of the first coordination polymer forming a coordination copolymer comprising at least a first region of the first coordination polymer and at least a second region of a second coordination polymer wherein the first coordination polymer is not identical to the second coordination polymer and wherein the x-ray diffraction pattern of the coordination copolymer comprises both the first x-ray diffraction pattern and the second x-ray diffraction pattern. 11. The method of claim 10 wherein the crystals of the first coordination polymer are of a size ranging from about 10 nanometers to about 1 micron. 12. The method of claim 10 wherein the treating of steps 10b and 10d comprise temperatures ranging from ambient to about 250° C. and reaction times from about 1 minutes to about 5 months. 13. The method of claim 10 wherein the treating of steps 10b and 10d comprise temperatures ranging from ambient to about 125° C. and reaction times from about 2 hours to about 4 days. 14. The method of claim 10 wherein the solvent is selected from the group consisting of formamides, sulfoxides, nitriles, esters, amines, ethers, ketones, aromatics, aliphatics, water, and combinations thereof. 15. The method of claim 10 further comprising: e) adding at least one additional reagent selected from the group consisting of a third source of metal cations, a third organic linking compound, and a combination thereof, to the solution or colloidal suspension;f) treating the solution or colloidal suspension to form crystals of a third coordination polymer as a layer over one or more crystals of the first coordination copolymer forming a second coordination copolymer wherein the third coordination polymer layer is not identical to the second coordination polymer. 16. The method of claim 15 wherein the third coordination polymer has the same composition and structure as the first coordination polymer. 17. The method of claim 15 further comprising: g) adding at least one additional reagent selected from the group consisting of an Nth source of metal cations, an Nth organic linking compound, and a combination thereof, to the solution or colloidal suspension, where N is an integer greater than 3;h) treating the solution or colloidal suspension to form crystals of a Nth coordination polymer as a layer over one or more crystals of the (N-1) coordination copolymer forming a coordination copolymer wherein the Nth coordination polymer layer is not identical to the (N-1) coordination polymer. 18. The method of claim 10 further comprising: i) adding the coordination copolymer of 10d) to a second solution or colloidal suspension of at least one source of metal cations and at least one organic linking compound solvent; andj) treating the second solution or colloidal suspension to form crystals of a third coordination polymer as a layer over one or more crystals of the coordination copolymer forming a second coordination copolymer wherein the third coordination polymer is not identical to the second coordination polymer. 19. The method of claim 18 wherein the third coordination polymer has the same composition and structure as the first coordination polymer.