Modified dense star polymers

Claim 2

An improved dense star polymer prepared in a reaction medium having at least one branch emanating from an immobilized core which core and its precursor are insoluble in the reaction medium in which the dense star polymer is prepared, said branch called a core branch having at least two terminal groups provided that (1) the ratio of terminal groups to the core branches is more than one, (2) the density of terminal groups per unit volume in the polymer is at least 1.5 times that of an extended conventional star polymer having similar core and monomeric moieties and a comparable molecular weight and number of core branches, each of such branches of the extended conventional star polymer bearing only one terminal group, and (3) a molecular volume that is no more than about 80 percent of the molecular volume of said extended conventional star polymer as determined by dimensional studies using scaled Core-Pauling molecular models.

Claim 3

The polymer of claim 1 wherein the core is derived from a cross-linked aromatic polymer.

Claim 4

The polymer of claim 2 wherein the aromatic polymer is a copolymer of styrene and divinylbenzene and the terminal groups of the dense star polymer are amine groups or carboxylic ester groups.

Claim 5

The polymer of claim 1 having a polyvalent core that is covalently bonded to at least two ordered dendritic (tree-like) branches which extend through at least two generations.

Claim 6

The polymer of claim 4 which has at least three ordered dendritic branches.

Claim 7

An excess reactant process for producing the dense star polymer of claim 1 comprising the steps of (A) contacting (1) an immobilized core compound having at least one nucleophilic or one electrophilic moiety called an N/E moiety with (2) an excess of a first organic coreactant having (a) a core-reactive moiety which is reactive with the N/E moieties of the immobilized core compound and (b) an N/E moiety which does not react with the N/E moiety of the core compound under conditions sufficient to form a core adduct wherein each N/E moiety of the core compound has reacted with the core reactive moiety of a different molecule of the first coreactant; (B) contacting (1) the core adduct having at least twice the number of N/E moieties as the core compound with (2) an excess of a second organic coreactant having (a) one moiety (hereinafter called an adjust reactive moiety) which will react with the N/E moieties of the core adduct and (b) a N/E moiety which does not react with the N/E moiety of the core adduct under conditions sufficient to form a first generation adduct having a number of N/E moieties that are at least twice the number of N/E moieties in the core adduct; and (C) contacting the first generation adduct with an excess of a third organic coreactant having one moiety that is reactive with the N/E moieties of the first generation adduct and an N/E moiety that does not react with the N/E moieties of the first generation adduct under conditions sufficient to form a second generation dendrimer.

Claim 8

The process of claim 6 wherein the immobilized core compound is a chloromethylated copolymer of styrene and divinylbenzene, the first organic coreactant is an alkylene polyamine, and the second organic coreactant is an acrylate ester.

Claim 9

The process of claim 7 wherein the alkylene polyamine is ethylenediamine and the second organic coreactant is methyl acrylate.

Claim 10

A partially protected reactant process for producing the dense star polymer of claim 1, wherein said dense star polymer is a polyamine, comprising the steps of (A) contacting (1) an immobilized core compound having at least one N/E moiety and (2) a first organic coreactant having a moiety which is reactive with the N/E moieties of the core compound and a blocking moiety, which does not react with the N/E moieties of the core compound, under conditions sufficient to form a blocked core adduct wherein each N/E moiety of the core compound has reacted with the reactive moiety of a different molecule of the first organic coreactant to form an adduct having block N/E moieties: (B) removing the blocking moieties from the blocked core adduct to form a first generation adduct having N/E moieties; (C) contacting (1) the first generation adduct which has at least twice the number of terminal N/E moieties as the core compound with (2) a second organic coreactant having a moiety which will react with the terminal N/E moieties of the first generation adduct and a blocking moiety (which does not react with the N/E moieties of the first generation adduct) under conditions sufficient to form a blocked second generation adduct having a number of blocked second generation adducts having a number of blocked N/E moieties that are at least twice the number of blocked N/E moieties in the blocked core adduct; and (D) removing the blocking moieties from the blocked second generation adduct to form a second generation adduct or dendrimer.