Organomodified siloxanes having primary amino functions, novel organomodified siloxanes having quaternary ammonium functions and the method for the production thereof

1. A method for producing selectively primary amino group-carrying siloxanes of general formula 1 or a quaternary ammonium derivative thereof, wherein

M a M′ a1 M″ a2 M′″ a3 D b D′ b1 D″ b2 D′″ b3 T c Q d    (formula 1)

where

M=(R 1 3 SiO 1/2 );

M′=(R 2 R 1 2 SiO 1/2 );

M″=(R 3 R 1 2 SiO 1/2 );

M′″=(R 4 R 1 2 SiO 1/2 );

D=(R 1 2 SiO 2/2 );

D′=(R 2 R 1 SiO 2/2 );

D″=(R 3 R 1 SiO 2/2 );

D′=(R 4 R 1 SiO 2/2 );

T=(R 5 SiO 3/2 );

Q=(SiO 4/2 );

a is in a range of from 0 to 32;

a1 is in a range of from 0 to 10;

a2 is in a range of from 0 to 32;

a3 is in a range of from 0 to 10;

b is in a range of from 0 to 600;

b1 is in a range of from 0.1 to 50;

b2 is in a range of from 0.1 to 20;

b3 is in a range of from 0 to 50;

c is in a range of from 0 to 20; and

d is in a range of from 0 to 20;

wherein:

if a1=2, at least one of b1, b2, b3, a2 and a3 is not 0 and at least two of the factors a2, a3, b1, b2 and b3 are not 0;

R 1 is each independently a linear or branched hydrocarbon radical having 1 to 30 carbon atoms or aromatic hydrocarbon radicals having 6 to 30 carbon atoms;

R 2 is each independently an organic radical comprising a primary amino function;

R 3 is each independently a radical selected from the group consisting of

—CH 2 —CH 2 —CH 2 —O—(CH 2 —CH 2 O—) x —(CH 2 —CH(R′)O—) y —R″,

—CH 2 —CH 2 —O—(CH 2 —CH 2 O—) x (CH 2 —CH(R′)O—) y —R″,

—CH 2 —CH 2 —(O) x′ —R IV ,

—CH 2 —CH 2 —CH 2 —O—CH 2 —CH(OH)—CH 2 OH, and

—CH 2 —CH 2 —CH 2 —O—CH 2 —C(CH 2 OH) 2 —CH 2 —CH 3 , wherein

x is in a range of from 0 to 100,

x′ is in a range of from 0 to 1,

y is in a range of from 0 to 100,

R′ is each independently a linear or substituted alkyl or aryl group having 1 to 12 carbon atoms, where, within at least one of a radical R 4 and a molecule of the formula 1, mutually different substituents R′ are optionally present, and

R″ is each independently a hydrogen radical or an alkyl group having 1 to 4 carbon atoms, or a group —C(O)—R′″ where R′″=an alkyl radical, a group —CH 2 —O—R′, an alkylaryl group, the group —C(O)NH—R′,

R IV is an optionally substituted hydrocarbon radical having 1 to 50 carbon atoms,

R 4 is each independently a linear, cyclic or branched, saturated or unsaturated or aromatic hydrocarbon radical having 1 to 30 carbon atoms which is optionally substituted with a group comprising heteroatoms O, N, S, P or halogen atoms and which optionally contains no primary or secondary amine functions, and

R 5 is each independently a radical of R 1 , R 2 , R 3 or R 4 , characterized in that

(a) laterally epoxy-modified siloxane of formula 3

M a M′″″ a1 M″ a2 M′″ a3 D b D′″″ b1 D″ b2 D′″ b3 T c Q d    (formula 3)

where:

M=(R 1 3 SiO 1/2 );

M′″″=(R 10 R 1 2 SiO 1/2 );

M″=(R 3 R 1 2 SiO 1/2 );

M′″=(R 4 R 1 2 SiO 1/2 );

D=(R 1 2 SiO 2/2 );

D′″″=(R 10 R 1 SiO 2/2 );

D″=(R 3 R 1 SiO 2/2 );

D′″=(R 4 R 1 SiO 2/2 );

T=(R 5 SiO 3/2 ); and

Q=(SiO 4/2 ),

where a, a1, a2, a3, b, b1, b2, b3, c, d, R 3 , R 4 and R 5 have the meaning as specified under formula 1 and

R 10 is each independently an organic epoxy radical

are reacted

(b) with ammonia or instead of ammonia, with an ammonium compound which is capable of producing ammonia,

(c) in the presence of a ring-opening catalyst or at a pressure 4 bar and above

(d) at a minimum temperature of 60° C. to 150° C.

2. The method according to claim 1 , wherein the epoxy-functional compound of the formula 3 comprises R 10 , wherein R 10 is each independently an organic epoxy radical selected from the group consisting of

3. The method according to claim 1 , wherein said ammonia or said ammonium compound used comprises one or more selected from the group consisting of gaseous ammonia, aqueous ammonia solutions, alcoholic ammonia solutions, ammonium halides, ammonium carbonate, hydrogencarbonate, ammonium sulfate, hydrogensulfate, ammonium sulfamate, ammonium phosphate, hydrogenphosphate, dihydrogenphosphate, ammonium cyanate, ammonium carboxylates, ammonium acetate, ammonium hydrogenoxalate, oxalate, ammonium hydrogencitrate, ammonium benzoate, ammonium formate, ammonium carbamate, ammonium lactate, ammonium tartrate, ammonium succinate, hydroxylamine, hydroxylamine-O-sulfonic acid, amidosulfonic acid and urotropin.

4. A method for producing selectively primary amino group-carrying siloxanes of general formula 1 or a quaternary ammonium derivative thereof, wherein

M a M′ a1 M″ a2 M′″ a3 D b D′ b1 D″ b2 D′″ b3 T c Q d    (formula 1)

where

M=(R 1 3 SiO 1/2 );

M′=(R 2 R 1 2 SiO 1/2 );

M″=(R 3 R 1 2 SiO 1/2 );

M′″=(R 4 R 1 2 SiO 1/2 );

D=(R 1 2 SiO 2/2 );

D′=(R 2 R 1 SiO 2/2 );

D″=(R 3 R 1 SiO 2/2 );

D′″=(R 4 R 1 SiO 2/2 );

T=(R 5 SiO 3/2 );

Q=(SiO 4/2 );

a is in a range of from 0 to 32;

a1 is in a range of from 0 to 10;

a2 is in a range of from 0 to 32;

a3 is in a range of from 0 to 10;

b is in a range of from 0 to 600;

b1 is in a range of from 0 to 50;

b2 is in a range of from 0.1 to 20;

b3 is in a range of from 0 to 50;

c is in a range of from 0 to 20; and

d is in a range of from 0 to 20;

wherein:

if a1=2, at least one of b1, b2, b3, a2 and a3 is not 0 and at least two of the factors a2, a3, b1, b2 and b3 are not 0;

R 1 is each independently a linear or branched hydrocarbon radical having 1 to 30 carbon atoms or aromatic hydrocarbon radicals having 6 to 30 carbon atoms;

R 2 is each independently an organic radical comprising a primary amino function;

R 3 is each independently a radical selected from the group consisting of

—CH 2 —CH 2 —CH 2 —O—(CH 2 —CH 2 O—) x —(CH 2 —CH(R′)O—) y —R″,

—CH 2 —CH 2 —O—(CH 2 —CH 2 O—) x (CH 2 —CH(R′)O—) y —R″,

—CH 2 —CH 2 —(O) x′ —R IV ,

—CH 2 —CH 2 —CH 2 —O—CH 2 —CH(OH)—CH 2 OH, and

—CH 2 —CH 2 —CH 2 —O—CH 2 —C(CH 2 OH) 2 —CH 2 —CH 3 , wherein

x is in a range of from 0 to 100,

x′ is in a range of from 0 to 1,

y is in a range of from 0 to 100,

R′ is each independently a linear or substituted alkyl or aryl group having 1 to 12 carbon atoms, where, within at least one of a radical R 4 and a molecule of the formula 1, mutually different substituents R′ are optionally present, and

R″ is each independently a hydrogen radical or an alkyl group having 1 to 4 carbon atoms, or a group —C(O)—R′″ where R′″=an alkyl radical, a group —CH 2 —O—R′, an alkylaryl group, the group —C(O)NH—R′,

R IV is an optionally substituted hydrocarbon radical having 1 to 50 carbon atoms,

R 4 is each independently a linear, cyclic or branched, saturated or unsaturated or aromatic hydrocarbon radical having 1 to 30 carbon atoms which is optionally substituted with a group comprising heteroatoms O, N, S, P or halogen atoms and which optionally contains no primary or secondary amine functions, and

R 5 is each independently a radical of R′, R 2 , R 3 or R 4 , characterized in that

(a) laterally epoxy-modified siloxane of formula 3

M a M′″″ a1 M″ a2 M′″ a3 D b D′″″ b1 D″ b2 D′″ b3 T c Q d    (formula 3)

where:

M=(R 1 3 SiO 1/2 );

M′″″=(R 10 R 1 2 SiO 1/2 );

M″=(R 3 R 1 2 SiO 1/2 );

M′″=(R 4 R 1 2 SiO 1/2 );

D=(R 1 2 SiO 2/2 );

D′″″=(R 10 R 1 SiO 2/2 );

D″=(R 3 R 1 SiO 2/2 );

D′″=(R 4 R 1 SiO 2/2 );

T=(R 5 SiO 3/2 ); and

Q=(SiO 4/2 ),

where a, a1, a2, a3, b, b1, b2, b3, c, d, R 3 , R 4 and R 5 have the meaning as specified under formula 1 and

R 10 is each independently an organic epoxy radical

are reacted

(b) with ammonia or instead of ammonia, with an ammonium compound which is capable of producing ammonia,

(c) in the presence of a ring-opening catalyst or at a pressure above 1 bar

(d) at a minimum temperature of 50° C. to 150° C.,

further comprising passing gaseous ammonia in a pressureless manner through a mixture comprising the epoxy-functional compound.

5. The method according to claim 1 , comprising carrying out the reaction at a pressure from 4 to 50 bar.

6. The method according to claim 1 , comprising carrying out the reaction at a pressure from 5-20 bar.

7. The method according to claim 1 , comprising carrying out the reaction at a pressure from 5-50 bar.