Tetra ketone porphyrin monomers and the process of preparation thereof

Claim 2

A tetraketone of structure: ##STR23## wherein M is a metal atom, and R is phenyl, alkyl substituted phenyl or halogen substituted phenyl.

Claim 3

The tetraketone I(a) of claim 1 wherein M is selected from copper, iron, nickel, cobalt or manganese.

Claim 4

The tetraketone of claim 2 wherein M is copper.

Claim 5

The tetraketone (I) of claim 1.

Claim 6

The tetraketone of claim 4 wherein R is phenyl.

Claim 7

A process for the preparation of a tetraketone of the structure: ##STR24## wherein R is selected from phenyl, alkyl substituted phenyl, or halogen substituted phenyl, which process comprises: (a) treating the chemical of the structure: ##STR25## with an oxidizing agent to remove any dihydrochlorin impurity and produce chemical II in at least 95% purity: (b) conducting the compound of step (a) with a metal salt to produce a porphyrin incorporating M; ##STR26## (c) contacting the purified chemical II(a) with N 2 O 4 to produce the dinitro-III(a) of the structure: ##STR27## (d) contacting the dinitro compound of step (c) with concentrated sulfuric acid to produce the dinitro demetallated compound III: ##STR28## (e) reducing the dinitro-III of step (d) with a reducing agent to produce the diamino-IV of the structure: ##STR29## (f) contacting the diamino-compound of step (e) with an oxidizing agent to produce the tetraketone of structure I.

Claim 8

A process for the preparation of a tetraketone of the structure: ##STR24## wherein R is selected from phenyl, alkyl substituted phenyl, or halogen substituted phenyl, which process comprises: (a) treating the chemical of the structure: ##STR25## with an oxidizing agent to remove any dihydrochlorin impurity and produce chemical II in at least 95% purity: (b) conducting the compound of step (a) with a metal salt to produce a porphyrin incorporating M; ##STR26## (c) contacting the purified chemical II(a) with N 2 O 4 to produce the dinitro-III(a) of the structure: ##STR27## (d) contacting the dinitro compound of step (c) with concentrated sulfuric acid to produce the dinitro demetallated compound III: ##STR28## (e) reducing the dinitro-III of step (d) with a reducing agent to produce the diamino-IV of the structure: ##STR29## (f) contacting the diamino-compound of step (e) with an oxidizing agent to produce the tetraketone of structure I.

Claim 9

The process of claim 6 wherein R is phenyl.

Claim 10

The process of claim 6 wherein M is copper cobalt.

Claim 11

The process of claim 6 which further includes: step (g) wherein the porphyrin of step (f) is contacted with a metal salt to produce the metal porphyrin compound of structure: ##STR30##

Claim 12

The process of claim 6 wherein in step (a) the oxidizing agent is dichlorodicyanoquinone, in step (b) the metal salt is selected from the group consisting of copper, iron, nickel, cobalt or manganese, in step (e) the reducing agent is palladium on carbon followed by sodium borohydride, and in step (f) the oxidizing agent is a combination of light energy and oxygen.

Claim 13

A process for the preparation of a tetraketone of the structure: ##STR31## wherein R is selected from phenyl, alkyl substituted phenyl, or halogen substituted phenyl, wherein M is a metal atom, which process comprises: (a) treating the chemical of the structure: ##STR32## with an oxidizing agent to remove any dihydrochlorin impurity and produce chemical II in at least 95% purity: (b) contacting the compound of step (a) with a metal salt to produce a porphyrin incorporating M; ##STR33## (c) contacting the purified chemical II(a) with N 2 O 4 to produce the dinitro-III(a) of the structure: ##STR34## (d) contacting the dinitro compound of step (c) with concentrated sulfuric acid to produce the dinitro demetallated compound III: ##STR35## (e) reducing the dinitro-III of step (d) with a reducing agent to produce the diamino-IV of the structure: ##STR36## (f) contacting the diamino-compound of step (e) with an oxidizing agent to produce the tetraketone of structure ##STR37## (g) contacting the porphyrin of step (f) with a metal salt to produce the metal porphyrin compound of structure Ia.

Claim 14

A process for the preparation of a tetraketone of the structure: ##STR31## wherein R is selected from phenyl, alkyl substituted phenyl, or halogen substituted phenyl, wherein M is a metal atom, which process comprises: (a) treating the chemical of the structure: ##STR32## with an oxidizing agent to remove any dihydrochlorin impurity and produce chemical II in at least 95% purity: (b) contacting the compound of step (a) with a metal salt to produce a porphyrin incorporating M; ##STR33## (c) contacting the purified chemical II(a) with N 2 O 4 to produce the dinitro-III(a) of the structure: ##STR34## (d) contacting the dinitro compound of step (c) with concentrated sulfuric acid to produce the dinitro demetallated compound III: ##STR35## (e) reducing the dinitro-III of step (d) with a reducing agent to produce the diamino-IV of the structure: ##STR36## (f) contacting the diamino-compound of step (e) with an oxidizing agent to produce the tetraketone of structure ##STR37## (g) contacting the porphyrin of step (f) with a metal salt to produce the metal porphyrin compound of structure Ia.

Claim 15

The process of claim 11 wherein R is phenyl.

Claim 16

The process of claim 11 wherein M is copper or cobalt.

Claim 17

The process of claim 11 wherein in step (a) the oxidizing agent is dichlorodicyanoquinone, in step (b) the metal salt is selected from the group consisting of copper, iron, nickel, cobalt or manganese, in step (e) the reducing agent is palladium on carbon followed by sodium borohydride, and in step (f) the oxidizing agent is a combination of light energy and oxygen.