All The Claims

1. A porous membrane for a secondary battery, comprising non-conductive particles and a binder for a porous membrane, wherein
the non-conductive particle is a polymer particle having a core-shell structure,
the non-conductive particle has a core portion having a glass transition point of 30\xb0 C. to 90\xb0 C.,
the non-conductive particle has a shell portion having a glass transition point higher than that of the core portion by 10\xb0 C. or higher,
a thickness of the shell portion is 0.01% to 3.0% of a number average particle diameter of the non-conductive particles, and
a number average particle diameter (A) of the non-conductive particle and a number average particle diameter (B) of the binder for a porous membrane satisfy (A)>(B).
2. The porous membrane for a secondary battery according to claim 1, wherein the shell portion of the non-conductive particles and the binder for a porous membrane contain 50% by weight or more of (meth)acrylate unit.
3. The porous membrane for a secondary battery according to claim 1, wherein the non-conductive particles have a number average particle diameter of 100 nm to 1,500 nm.
4. A method for producing the porous membrane for a secondary battery according to claim 1, comprising:
mixing the non-conductive particles, the binder for a porous membrane, and a medium to prepare a slurry for a porous membrane;
applying the slurry for a porous membrane onto a substrate to form a slurry layer; and
drying the slurry layer.
5. The method according to claim 4, wherein
the medium is an aqueous medium, and
the slurry for a porous membrane is an aqueous dispersion.
6. An electrode for a secondary battery, comprising:
a current collector;
an electrode material layer that contains an electrode active material and a binding agent for an electrode material layer, and adheres to the current collector, and
the porous membrane according to claim 1 that is formed on the electrode material layer.
7. A separator for a secondary battery, comprising:
an organic separator; and
the porous membrane according to claim 1 that is formed on the organic separator.
8. A secondary battery comprising a positive electrode, a negative electrode, a separator, and an electrolytic solution, wherein
at least any one of the positive electrode, the negative electrode, and the separator has the porous membrane according to claim 1.
The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A compound of the formula I

112
in which:
W is R1ABDC(R16), R1ABDC(R16)C,

113
with it being possible for the ring systems

114
to contain 1 or
2 heteroatoms from the group N, O and S, to be saturated or unsaturated, once or more than once, and be substituted by 1-3 substituents from R16 or substituted, once or twice, by doubly bonded O or S;
Y is CO, CS or CH2;
Z is N(R0), O, S or CH2;
A is a direct linkage, (C1-C8)-alkanediyl, NR2NCR2, NR2C(O)NR2, NR2C(O)O, NR2C(O)S, NR2C(S)NR2, NR2C(S)O, NR2C(S)S, NR2S(O)nNR2, NR2S(O)nO, NR2S(O)n, (C3-C12)-cycloalkanediyl, CC, NR2C(O), C(O)NR2, (C5-C14)-arylene-C(O)NR2, O, S(O), (C5-C14)-arylene-, CO, (C5-C14)-arylene-CO, NR2, SO2NR2,C(O)O, OC(O), NCR2, R2CN, CR2CR3or (C5-C14)-arylene-S(O)n, which in each case can be substituted by NR2 andor substituted, once or twice, by (C1-C8)-alkanediyl;
B is a direct linkage, (C1-C8)-alkanediyl, (C5-C10)-arylene, (C3-C8)-cycloalkanediyl, CC, NR2, C(O), NR2C(O), C(O)NR2, NR2C(O)NR2, NR2C(S)NR2, OC(C), C(O)O, S(C), S(O)2, S(O)NR2, S(O)2NR2, NR2S(O), NR2S(O)2, O, S or CR2CR3, which in each case can be substituted once or twice by (C1-C6)-alkanediyl, or is a divalent radical of a 5- or 6-membered saturated or unsaturated ring which contains 1 or 2 nitrogen atoms and can be substituted, once or twice, by (C1-C6)-alkyl or doubly bonded oxygen or sulfur;
D is a direct linkage, (C1-C8)-alkanediyl, (C5-C10)-arylene, O, NR2, CONR2, NR2CO, NR2C(O)NR2, NR2C(S)NR2, OC(O), C(O),CO,CS, S(O), S(O)2, S(O)2NR2, NR2S(O), NRS(O)2, S, CRCR, CC, NR2NCR2, NCR2, R2CN or CH(OH), which in each case can be substituted, once or twice, by (C1-C8)-alkanediyl, CR2CR3or (C5-C6)-arylene;
E is a direct linkage, (C1-C6)-alkanediyl, (C2-C6)-alkenediyll, (C2-C6)-alkynediyl, phenylene, phenylene-(C1-C3)-alkanediyl or (C1-C3)-alkanediyl-phenylene;
F is defined as D;
G is

115
L is C(R16) or N;
R0 is H, (C1-C8)-alkyl which is optionally substituted, once or more than once, by fluorine, (C3-C12)-cycloalkyl, (C3-C12)-cycloalkyl-(C1-C8)-alkyl, (C1-C14)-aryl, (C5-C14 )-aryl-(C1-C8)-alkyl or (C1-C8)-alkyl-C(O), (C3-C12)-cycloalkyl-C(O), (C3-C12)-cycloalkyl-(C1-C6)-alkyl-C(O), (C5-C14)-aryl-C(O) or (C5-C14)-aryl-(C1-C6)-alkyl-C(O), with it being possible for the alkyl radicals to be substituted, once or more than once, by fluorine;
R1 is R2C(NR2)NR2, R2R3NC(NR2), R2R3NC(NR2)NR, or a 4 to 14-membered, monocyclic or polycyclic, aromatic or non-aromatic ring system which can optionally contain 1-4 heteroatoms from the group N, O and S and can optionally be substituted, once or more than once, by substituents from the group R12, R13, R14 and R15;
R2 and R3 are, independently of each other, H, (C1-C10)-alkyl, which is optionally substituted, once or more than once, by fluorine, (C3-C12)-cycloalkyl, (C3-C12)-cycloalkyl-(C1-C8)-alkyl, (C5-C14)-aryl, (C5-C14)-aryl-(C1-C8)-alkyl, H2N, R8ONR9, R8OR9, R6OC(O)R9, R8(C5-C14)-aryl-R9, R8R8NR9, HO(C1-C8)-alkyl-NR8R9, R8R8NC(O)R9, R8C(O)NR8R9, R8C(O)R9, R8R8NC(NR8), R8R8NC(NR8)NR8 or (C1-C18)-alkylcarbonyloxy-(C1-C6)-alkoxycarbonyl;
R4, R5, R6 and R7 are, independently of each other, H, fluorine, OH, (C1-C8)-alkyl, (C3-C12)-cycloalkyl, (C3-C12)-cycloalkyl-(C1-C8)-alkyl, or R8OR9, R3SR9, R8CO2R9, R8OC(O)R9, R8(C5-C14)-aryl-R9, R8N(R2)R9, R8R8NR9, R8N(R2)C(O)OR9, R8S(O)nN(R2)R9, R8OC(O)N( R2)R9, to R8N(R2)C(O)N(R2)R9, R8N(R2)S(O)nN(R2)R9, R8S(O)nR9, R8SC(O)N(R2)R9, R8C(O)R9, R8N(R2)C(O)R9 or R8N(R2)S(O)nR9;
R8 is H, (C1-C8)-alkyl, (C3-C12)-cycloalkyl, (C3-C12)-cycloalkyl-(C1-C8)-alkyl, (C5-C14)-aryl or (C5-C14)-aryl-(C1-C8)-alkyl, with it being possible for the alkyl radicals to be substituted, once or more than once, by fluorine;
R9 is a direct linkage or (C1-C8)-alkanediyl;
R10 is C(O)R11, C(S)R11, S(O)nR11, P(O)nR11 or a four- to eight-membered, saturated or unsaturated heterocycle which contains 1, 2, 3 or 4 heteroatoms from the group N, O and S;
R11 is OH, (C1-C8)-alkoxy, (C5-C14)-aryl-(C1-C8)-alkoxy, (C5-C14)-aryloxy, (C1-C8)-alkylcarbonyloxy-(C1-C4)-alkoxy, (C5-C14)-aryl-(C1-C8)-alkylcarbonyloxy-(C1-C6)-alkoxy, NH2, mono- or di(C1-C8-alkyl)amino, (C5-C14)-aryl-(C1-C14)-alkylamino, (C1-C8)-dialkylamino-carbonylmethyloxy, (C5-C14)-aryl-(C1-C8)-dialkylaminocarbonylmethyloxy or (C5-C14)-arylamino or an L- or D-armino acid;
R12, R13, R14 and R15 are, independently of each other, H, (C1-C10)-alkyl which is optionally substituted, once or more than once, by fluorine, (C3-C12)-cycioalkyl, (C3-C12)-cycloalkyl-(C1-C8)-alkyl, (C5-C14)-aryl, (C5-C14)-aryl-(C1-C8)-alkyl, H2N, R8ONR9, R8OR9, R8OC(O)R9, R8R8NR9, R8(C5-C14)-aryl-R9, HO(C1-C8)-alkyl-N(R2)R9, R8N(R2)C(O)R9, R8C(O)N(R2)R9, R8C(O)R9, R2R3NC(NR2)NR2, R2R3NC(NR2), O or S; with it being possible for two adjacent substituents from the group R12 to R15 also together to be OCH2O, OCH2CH2O or OC(CH3)2O;
R16 is H, (C1-C10)-alkyl which is optionally substituted, once or more than once, by fluorine, (C3-C12)-cycloalkyl, (C3-C12)-cycloalkyl-(C1-C8)-alkyl, (C5-C14)-aryl, (C5-C14)-aryl-(C1-C8)-alkyl, (C2-C20)-alkenyl or (C2-C10)-alkynyl;
m is 1, 2, 3, 4, 5 or 6;
n is 1 or 2;
p and q are, independently of each other, 0 or 1; and the physiologically tolerated salts thereof,
with compounds being excluded in which R1ABDC(R16) or R1ABDC(R16)C is R1KC(R16) or R1KCHC (R16H), where, in this case,
R1 is XNHC(NH)(CH2)p, X1(NH(CH2)p or 4-imidazolyl-CH2, wherein p is an integer from 0 to 3,
X is hydrogen, (C1-C6)-alkyl, (C1-C6)-alkylcarbonyl, (C1-C6)-alkoxycarbonyl, (C1-C18)-alkylcarbonyloxy-(C1-C6)-alkoxycarbonyl, (C6-C14)-arylcarbonyl, (C6-C14)-aryloxycarbonyl, (C6-C14)-aryl-(C1-C6)-alkoxycarbonyl, hydroxyl, (C1-C6)-alkoxy, (C6-C14)-aryl-(C1-C6)-alkoxy or amino, with the aryl groups in X being pure carbocycies which are optionally substituted once or more than once.
X1 is (C4-C14)-arylcarbonyl, (C4-C14)-aryloxycarbonyl, (C4-C14)-aryl-(C1-C6)-alkoxycarbonyl, (C4-C14)-aryl-(C1-C6)-alkoxy or RNHC(NR), where R and R have, independently of each other, the meanings of X and where the aryl groups in X1 are pure carbocycles which are optionally substituted once or more than once,
K is (C1-C6)-alkanediyl, (C3-C7)-cycloalkanediyl, phenylene, phenylene-(C1-C6)-alkanediyl, (C1-C6)-alkanediylphenylene, phenylene-(C2-C6)-alkenediyl or a divalent radical of a 5- or 6-membered, saturated or unsaturated ring which contains 1 or 2 nitrogen atoms and can be substituted, once or twice, by (C1-C6)-alkyl or doubly bonded oxygen or sulfur.
2. A compound of the formula I as claimed in claim 1 in which:
W is RABDC(R16), R1ABDC(R16)C,

116
where the ring systems

117
contain 1 or 2 heteroatoms from the group N and O, can be saturated or unsaturated once, and can be substituted by 1 or 2 substituents from R16;
Y is CO, CS or CH2;
Z is N(R0), O or CH2;
A is a direct linkage, (C1-C6)-alkanediyl, NR2NCR2, NR2C(O)NR2, NR2C(O)O, NR2C(O)S, NR2C(S)NR2, NR2C(S)O, NR2C(S)S, NR2S(O),NR2, NR2S(O)nO, NR2S(O)n, (C3-C8)-cycloalkanediyl, CC, NR2C(O), C(O)NR2, (C5-C12)-arylene-C(O)NR2, O, S(O)n, (C5-C12)-arylene-, CO, (C5-C12)-arylene-CO, NR2, SO2NR2, C(O)O, OC(O), NCR2, R2CN, CR2CR3, (C5-C12)-arylene-S(O)n, which in each case can be substituted by NR2 andor be substituted, once or twice, by (C1-C8)-alkanediyl;
B is a direct linkage, (C1-C6)-alkanediyl, (C5-C8)-arylene, (C3-C8)-cycloalkanediyl, CC, NR2, C(O), NR2C(O), C(O)NR2, NR2C(O)NR2, S(O), S(O)2, S(O)NR2, S(O)2NR2, NR2S(O), NR2S(O)2, O, CR2CR3, which in each case can be substituted, once or twice, by (C1-C6)-alkanediyl;
D is a direct linkage, (C1-C8)-alkanediyl, (C5-C8)-arylene, O, NR2, CONR2, NR2CO, NR2C(O)NR2, NR2C(S)NR2, OC(O), C(O)O, CO, CS, S(O), S(O)2, S(O)2NR2, NR2S(O), NR2S(O)2, S, CR2CR3, CC, NR2NCR2, NCR2, or R2CN, which in each case can be substituted, once or twice, by (C1-C6)-alkanediyl, CR2CR3 or (C5-C6)-arylene;
E is a direct linkage, (C1-C4)-alkanediyl, (C2-C4)-alkenediyl, (C2-C4)-alkynediyl, phenylene, phenylene-(C1-C2)-alkanediyl or (C1-C2)-alkanediylphenylene;
F is defined as D;
G is

118
L is C(R16) or N;
R0 is H, (C1-C6)-alkyl, (C3-C8)-cycloalkyl, (C3-C8)-cycloalkyl-(C1-C6)-alkyl, (C5-C12)-aryl, (C5-C12)-aryl-(C1-C6)-alkyl, (C1-C8)-alkyl-C(O), (C3-C8)-cycloalkyl-C(O), (C3-C8)-cycloalkyl-(C1-C4)-alkyl-C(O), (C5-C12)-aryl-C(O) or (C5-C12)-aryl-(C1-C14)-alkyl-C(O), where the alkyl radicals can be substituted, once or more than once, by fluorine;
R1 is R2C(NR2)NR3, R2R3NC(NR2), R2R3NC(NR2)NR2, or a 4-10-membered, monocyclic or polycyclic, aromatic or non-aromatic ring system which can optionally contain 1-4 heteroatoms from the group N, O and S and can optionally be substituted, once or more than once, by substituents from the group R12, R13, R14 and R15;
R2 and R3 are, independently of each other, H, (C1-C8)-alkyl which is optionally substituted, once or more than once, by fluorine, (C3-C8)-cycloalkyl, (C3-C8)-cycloalkyl-(C1-C6)-alkyl, ( C5-C12)-aryl, (C5-C12)-aryl-(C1-C6)-alkyl, H2N, R8ONR9, R8OR9, R8OC(O)R9, R8(C5-C12)-aryl-R9, R8R8NR9, HO(C1-C8)-alkyl-NR8R9, R8R8NC(O)R9, R8C(O)NR8R9, R8C(O)R9, R8R8NC(NR8), R8R8NC(NR8)NR8 or (C1-C10)-alkylcarbonyloxy-(C1-C4)-alkoxycarbonyl;
R4, R5, R6 and R7 are, independently of each other, H, fluorine, OH, (C1-C8)-alkyl, (C5-C12)-cycloalkyl, (C5-C12)-cycloalkyl-(C1-C8)-alkyl, or R8OR9, R8SR9, R8CO2R9, R8OC(O)R9, R8(C5-C12)-aryl-R9, R8N(R2)R9, R8R8NR9, R8N(R2)C(O)OR9, R8S(O)nN(R2)R9, R8OC(O)N(R2)R9, R8C(O)N(R2)R9, R8N(R2)C(O)N(R2)R9, R8N(R2)S(O)nN(R2)R9, R8S(O)nR9, R8SC(O)N(R2)R9, R8C(O)R9, R8N(R2)C(O)R9, R8N(R2)S(O)nR9;
R8 is H, (C1-C6)-alkyl, (C5-C12)-cycloalkyl, (C5-C12)-cycloalkyl-(C1-C6)-alkyl, (C5-C12)-aryl or (C5-C12)-aryl-(C1-C6)-alkyl, where the alkyl radicals can be substituted, once or more than once, by fluorine;
R9 is a direct linkage or (C1-C6)-alkanediyi;
R10 is C(O)R11, C(S)R11, S(O)nR11, P(O)nR11 or a 4- to 8-membered, saturated or unsaturated heterocycle which contains 1, 2, 3 or 4 heteroatoms from the group N, O and S;
R11 is OH, (C1-C6)-alkoxy, (C5-C12)-aryl-(C1-C6)-alkoxy, (C5-C12)-aryloxy, (C1-C6)-alkylcarbonyloxy-(C1-C4)-alkoxy, (C5-C12)-aryl-(C1-C6)-alkylcarbonyloxy-(C1-C6)-alkoxy, NH2, mono- or di(C1-C6-alkyl)amino, (C5-C12)-aryl-(C1-C6)-alkylamino or (C1-C6)-dialkylaminocarbonylmethyloxy;
R12, R13, R14 and R15 are, independently of each other, H, (C1-C8)-alkyl, which is optionally substituted, once or more than once, by fluorine, (C3-C8)-cycloalkyl, (C3-C8)-cycloalkyl-(C1-C6)-alkyl, (C5-C12)-aryl, (C5-C12)-aryl-(C1-C6)-alkyl, H2N, R8ONR9, R8OR9, R8OC(O)R9, R8(C5-C12)-aryl-R9, R8R8NR9, HO(C1-C8)-alkyl-N(R2)R9, R8N(R2)C(O)R9, R8C(O)N(R2)R9, R8C(O)R9, R2R3NC(NR2), R2R3NC(NR3)NR2, O or S; where two adjacent substituents from the group R12 to R15 can also together be OCH2O, OCH2CH2O or OC(CH3)2O;
R16 is H, (C1-C8)-alkyl which is optionally substituted, once or more than once, by fluorine, (C3-C8)-cycloalkyl, (C3-C8)-cycloalkyl-(C1-C6)-alkyl, (C5-C12)-aryl, (C5-C12)-aryl-(C1-C6)-alkyl, (C2-C8)-alkenyl or (C2-C8)-alkynyl;
m is 3,4 or 5;
n is 1 or 2; and
p and q are, independently of each other, 0 or 1. And the physiologically tolerated salts thereof.
3. A compound of the formula I as claimed in claim 1 in which:
W is R1AEDC(R16), R1ABDC(R16)C or

119
Y is CO, CS or CH2;
Z is N(R0) or CH2;
A is a direct linkage, (C1-C6)-alkanediyl, NR2NCR2, NR2C(O)NR2, NR2C(O)O, NR2C(O)S, NR2S(O)NNR2, NR2S(O)n, (C3-C6)-cycloalkanediyl, CC, NR2C(O), C(O)NR2, (C5-C10)-arylene-C(O)NR2, O, (C5-C10)-arylene-, CO, (C5-C10 )-arylene-CO, NR2, C(O)O, NCR2, R2CN or CR2CR3, which in each case can be substituted by NR2 andlor be substituted, once or twice, by (C1-C6)-alkanediyl;
B is a direct linkage, (C1-C6)-alkanediyl, (C5-C6)-arylene, (C5-C6)-cycloalkanediyl, CC, NR2C(O), C(O)NR2, NR2S(O)2, O or CR2CR3, which in each case can be substituted, once or twice, by (C1-C6)-alkanediyl;
D is a direct linkage, (C1-C6)-alkanediyl, (C5 -C6)-arylene, O, NR2, NR2CO, NR2C(O)NR2, NR2C(S)NR2, OC(O), C(O), S(O)2NR2, NR2S(O), NR2S(O)2, NCR2 or R2CN, which in each case can be substituted, once or twice, by (C1-C6)-alkanediyl;
E is a direct linkage, (C1-C4)-alkanediyl or (C2-C4)-alkenediyl;
F is a direct linkage, (C1-C6)-alkanediyl, O, CONR2, NR2CO, NR2C(O)NR2, OC(O), C(O)O, CO, S(O)2, S(O)2NR2, NR2S(O)2, CR2CR3, CC, NCR2 or R2CN, which in each case can be substituted, once or twice, by (C1-C6)-alkanediyl;
G is

120
L is C(R16) or N;
R0 is H, (C1-C6)-alkyl, (C3-C6)-cycloalkyl, (C3-C6)-cycloalkyl-(C1-C4)-alkyi, (C5-C10)-aryl, (C5-C10)-aryl-(C1-C4)-alkyl, (C1-C6)-alkyl-C(O), (C5-C6)-cycloalkylmethyl-C(O), phenyl-C(O) or benzyl-C(O), where the alkyl radicals can be substituted by 1-6 fluorine atoms;
R1 is R2C(NR2)NR2, R2R3NC(NR2),

121
with Y being NR2, O or S.
R2 and R3 are, independently of each other, H, (C1-C6)-alkyl which is optionally substituted, once or more than once, preferably 1-6 times, by fluorine, (C3-C6)-cycloalkyl, (C3-C6)-cycloalkyl-(C1-C4)-alkyl, (C5-C10)-aryl, (C5-C10)-aryl-(C1-C4)-alkyl, H2N, R8OR9, R8(C5-C10)-aryl-R9, R8NHR9, R8R8NR9, R8NHC(O)R9, R8C(O), H2NC(NH) or H2NC(NH)NH;
R4, R5, R6 and R7 are, independently of each other, H, fluorine, OH, (C1-C6)-alkyl, (C6-C12)-cycloalkyl, (C6-C12)-cycloalkyl-(C1-C6)-alkyl, or R8OR9, R8CO2R9, R8OC(O)R9, R8-(C5-C10)-aryl-R9, R8NHR9, R8R8NR9, R8NHC(O)OR9, R8S(O)nNHR9, R8OC(O)NHR9, R8C(O)NHR9, R8C(O)R9, R8NHC(O)NHR9, R8NHS(O)nNHR9, R8NHC(O)R9, R8NHS(O)nR9;
R8 is H, (C1-C6)-alkyl, (C6-C12)-cycloalkyl, (C6-C12)-cycloalkyl-(C1-C4)-alkyl, (C5-C10)-aryl or (C5-C10)-aryl-(C1-C4)-alkyl, where the alkyl radicals can be substituted by 1-6 fluorine atoms;
R9 is a direct linkage or (C1-C6)-alkanediyl;
R10 is C(O)R11, S(O)nR11 or P(O)nR11:
R11 is OH, (C1-C6)-alkoxy, (C5-C10)-aryl-(C1-C6)-alkoxy, (C5-C10)-aryloxy, (C1-C6)-alkylcarbonyloxy-(C1-C4)-alkoxy, (C5-C10)-aryl-(C1-C4)-alkylcarbonyloxy-(C1-C4)-alkoxy, NH2 or mono- or di(C1-C6-alkyl)-amino;
R12, R13 and R14 are H, (C1-C6)-alkyl, which is optionally substituted, once or more than once, by fluorine, (C3-C6)-cycloalkyl, (C3-C6)-cycloalkyl-(C1-C4)-alkyl, (C5-C10)-aryl, (C5-C10)-aryl-(C1-C4)-alkyl, H2N, R8OR9, R8OC(O)R9, R8-(C5-C10)-aryl-R9, R8R8NR9, R8NHC(O)R9, R8C(O)NHR9, H2NC(NH), H2NC(NH)NH or O; where two adjacent substituents from the group R12 to R14 can also together be OCH2O or OCH2CH2O;
R16 is H, (C1-C6)-alkyl which can be substituted 16 times by fluorine, (C3-C6)-cycloalkyl, (C3-C6)-cycloalkyl-(C1-C4)-alkyl, phenyl, phenyl-(C1-C4)-alkyl or (C2-C6)-alkenyl;
m is 3,4 or 5;
n is 1 or 2; and
p and q are, independently of each other, 0 or 1, and the physiologically tolerated salts thereof.
4. A compound of the formula I as claimed in claim 1 , in which:
W is R1AEDC(R16) or R1ABDCHC,
Y is CO or CS;
Z is N(R0);
A is a direct linkage, (C1-C4)-alkanediyl, NR2NCR2, NR2C(O)NR2, NR2C(O)O, NR2S(O)n, NR2S(O)nNR2, NR2CO, NR2 or NCR2, which in each case can be substituted by NH andor be substituted, once or twice, by (C1-C4)-alkanediyl;
B is a direct linkage, (C1-C4)-alkanediyl, phenylene, a divalent radiical of pyridine, thiophene or furane, cyclohexanediyl, CC, CR2CR3, C(O)NR2 or NR2C(O), which in each case can be substituted, once or twice, by (C1-C4)-alkanediyl;
D is a direct linkage, (C1-C4)-alkanediyl, phenylene, O, NR2, NR2CO, NR2C(O)NR2, R2NS(O)2NR2, NR2S(O)2, NR2S(O), NCR2 or R2CN, which in each case can be substituted, once or twice, by (C1-C4)-alkanediyl;
E is a direct linkage or (C1-C4)-alkanediyl;
F is a direct linkage, (C1-C6)-alkanediyl, O, CONR2, NR2CO, NR2C(O)NR2, S(O)2NR2, NR2S(O)2, CR2CR3, CC, NCR2 or R2CN, which in each case can be substituted, once or twice, by (C1-C4)-alkanediyl;
G is

122
R0 is H, (C1-C6)-alkyl, trifluoromethyl, pentafluoroethyl, (C5-C6)-cycloalkyl, (C5-C6)-cycloalkyl-(C1-C2)-alkyl, optionally substituted phenyl or benzyl which is optionally substituted on the phenyl radical;

123
R2 and R3 are, independently of each other, H, (C1-C6)-alkyl, trifluoromethyl, pentafluoroethyl, (C5-C6)-cycloalkyl, (C5-C6)-cycloalkyl-(C1-C2)-alkyl, phenyl, benzyl, H2N, R8OR9, R8(C5-C10)-aryl-R9, R8NHR9, R8R8NR9, R8NHC(O)R9, H2NC(NH) or H2CC(NH)NH;
R4, R5, R8 and R7 are, independently of each other, H, fluorine, OH, (C1-C6)-alkyl, (C10-C12)-cycloalkyl, (C10-C12)-cycloalkyl-(C1-C6)-alkyl, or R80R9, R8-(C5-C10)-aryl-R9, R8R8NR9, R8NHC(O)OR9, R8S(O)nNHR9, R8OC(O)NHR9 or R8C(O)NHR9;
R8 is H, (C1-C6)-alkyl, (C10-C12)-cycloalkyl, (C10-C12)-Cycloalkyl-(C1-C2)-alkyl, (C5-C10)-aryl or (C5-C10)-aryl-(C1-C2)-alkyl;
R9 is a direct linkage or (C1-C6)-alkanediyl,
R10 is C(O)R11;
R11 is OH, (C1-C6)-alkoxy, phenoxy, benzyloxy, (C1-C4)-alkylcarbonyloxy-(C1-C4)-alkoxy, NH2, mono- or di(C1-C8-alkyl)amino;
R16 is H, (C1-C4)-alkyl, trifluoromethyl, pentafluoroethyl, (C5-C6)-cycloalkyl, (C5-C6)-cycloalkyl-(C1-C2)-alkyl, phenyl or benzyl;
n is 1 or 2; and
p and q are, independently of each other, 0 or 1, and the physiologically tolerated salts thereof.
5. A process for preparing a compound of formula I as claimed in claim 1 wherein F is C(O)NR2, comprising linking a compound of formula II

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wherein M is hydroxycarbonyl, (C1-C6)-alkoxycarbonyl, or an activated carboxylic acid derivative, and W, Z, Y, and E are as defined in claim 1, with HNR2G, wherein G and R2 are as defined in claim 1.
6. A pharmaceutical composition comprising a vitronectin receptor antagonistic amount of the compound of claim 1, and a pharmaceutically acceptable carrier.
7. A method of treating a disease or condition associated with vitronectin receptor binding comprising administering to a mammal the composition of claim 6.
8. A method of treating a disease or condition associated with the interaction between vitronectin receptors and their ligands in cell-cell or cell-matrix interaction processes, comprising the administration of the compound of claim 1 to a mammal, wherein said disease or condition is selected from the group consisting of reabsorption by osteoclasts, tumor growth and tumor metastasis, inflammation, cardiovascular disease, nephropathies and retinopathies.

1. A touch sensor assembly comprising:
a touch sensor overlay comprising a plurality of touch sensitive elements and a plurality of conductors connected to the touch sensitive elements arranged on the touch sensor periphery; and
a frame subassembly affixed to the touch sensor periphery, the frame subassembly comprising a frame and one or more circuit boards held in place by the frame, the one or more circuit boards electrically connected to the plurality of conductors,
wherein the circuit boards include circuitry for conditioning signals communicated by the touch sensitive elements due to a touch on the touch sensor overlay.
2. The touch sensor assembly of claim 1, wherein the touch sensor overlay comprises one or more flexible films laminated to a rigid substrate, the plurality of touch sensitive elements and the plurality of conductors being formed on the flexible film.
3. The touch sensor assembly of claim 2, wherein the frame has a coefficient of thermal expansion that falls within a range bounded by the coefficients of thermal expansion of the one or more flexible films and the rigid substrate.
4. The touch sensor assembly of claim 1, wherein the frame comprises a glass filled liquid crystal polymer or a glass filled polycarbonate.
5. The touch sensor assembly of claim 1, wherein frame subassembly is affixed to the touch sensor by a pressure sensitive adhesive, the pressure sensitive adhesive having apertures in each of which is placed a conductive material to electrically connect the one or more circuit boards to the plurality of conductors.
6. The touch sensor assembly of claim 1, wherein frame subassembly is affixed to the touch sensor by a z-axis conductive adhesive that functions to electrically connect the one or more circuit boards to the plurality of conductors.
7. The touch sensor assembly of claim 1, wherein the frame subassembly further comprises self-fixturing features.
8. The touch sensor assembly of claim 7, wherein the self-fixturing features include alignment tabs extending from the plane of the frame.
9. The touch sensor assembly of claim 7, wherein the self-fixturing features determine a spacing between one or more of the frame and a part of the touch sensor, the frame and the one or more circuit boards, and the one or more circuit boards and a part of the touch sensor.
10. A method of bonding electronics to a touch sensitive overlay comprising the steps of:
providing a touch sensor comprising a plurality of touch sensitive elements and a plurality of conductors connected to the touch sensitive elements arranged on the touch sensor periphery;
providing one or more circuit boards that include circuitry for conditioning signals communicated by the touch sensitive elements due to a touch on the touch sensor, each circuit board having a plurality of conductive contact areas;
dispensing an insulative adhesive on the touch sensor periphery and forming apertures in the adhesive to individually expose the plurality of conductors on the touch sensor;
placing a conductive material on the plurality of conductors; and
positioning the one or more circuit boards on the touch sensor periphery so that the conductive material electrically connects each of the conductive contact areas to one of the plurality of conductors, and the adhesive bonds the circuit board to the touch sensor.
11. The method of claim 10, further comprising using a frame to aid in the positioning of the one or more circuit boards.
12. The method of claim 11, further comprising providing self-fixturing features on the frame to control a spacing of one or more of:
a. the one or more circuit boards and a part of the touch sensor;
b. the frame and part of the touch sensor; and
c. the frame and the one or more circuit boards.
13. The method of claim 11, wherein the frame has a coefficient of thermal expansion that closely matches the coefficient of thermal expansion of the touch sensor materials.
14. The method of claim 10, wherein the step of dispensing and forming apertures in the adhesive is performed prior to placing the conductive material on the plurality of conductors.
15. The method of claim 10, wherein the step of placing the conductive material on the plurality of conductors is performed prior to dispensing and forming apertures in the adhesive.
16. The method of claim 10, wherein the step of dispensing and forming apertures in the adhesive comprises forming the apertures in a pressure sensitive adhesive layer and adhering the pressure sensitive adhesive layer to the touch sensor periphery.

The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.

1. A 3D image reproduction apparatus, comprising:
an acquisition section that acquires video image data configured from a right eye image and a left eye image for displaying a 3D image, image capture shortest distance data representing an image capture shortest distance during image capture of the video image data, image capture data for computing distance, and parallax data representing a setting parallax that is set for the right eye image and the left eye image;
a computation section that detects a predetermined main imaging subject in each frame of the video image data, that computes a main imaging subject parallax for each of the frames based on the detected main imaging subject, and that employs the image capture data and the setting parallax to compute a relationship between the main imaging subject parallax and a main imaging subject distance; and
an adjustment section that, when the image capture shortest distance data has been acquired by the acquisition section, adjusts the setting parallax acquired by the acquisition section such that a maximum parallax of the main imaging subject is within a predetermined permissible range when image capture was at the image capture shortest distance, using the relationship between the main imaging subject parallax and the main imaging subject distance that has been computed by the computation section.
2. The 3D image reproduction apparatus of claim 1, wherein the computation section performs computation of the main imaging subject parallax and computation of the relationship between the main imaging subject parallax and the main imaging subject distance at least on a first frame containing the main imaging subject.
3. The 3D image reproduction apparatus of claim 1, wherein, when the image capture shortest distance data is not acquired by the acquisition section, the adjustment section adjusts the setting parallax such that the maximum parallax is in the permissible range even when an imaging subject approaches to immediately in front of an image capture device for capturing the video image.
4. The 3D image reproduction apparatus of claim 1, wherein the adjustment section shifts horizontal direction display positions of a right eye image and a left eye image of each of the frames such that the maximum parallax is within the permissible range.
5. A parallax adjustment method for a 3D image reproduction apparatus, the method comprising:
acquiring video image data configured from a right eye image and a left eye image for displaying a 3D image, image capture shortest distance data representing an image capture shortest distance during image capture of the video image data, image capture data for computing distance, and parallax data representing a setting parallax that is set for the right eye image and the left eye image;
computing a main imaging subject parallax for each of the frames based on a main imaging subject detected by detecting a predetermined main imaging subject in each frame of the video image data, and computing a relationship between the main imaging subject parallax and a main imaging subject distance by employing the image capture data and the setting parallax; and
when the image capture shortest distance data has been acquired, adjusting the acquired setting parallax such that a maximum parallax of the main imaging subject is within a predetermined permissible range for image capture at the acquired image capture shortest distance, using the computed relationship between the main imaging subject parallax and the main imaging subject distance.
6. The parallax adjustment method for a 3D image reproduction apparatus of claim 5, wherein computation of the relationship between the main imaging subject and the main imaging subject distance is performed at least on a first frame containing the main imaging subject.
7. The parallax adjustment method for a 3D image reproduction apparatus of claim 5, wherein when the image capture shortest distance data is not acquired, the setting parallax is adjusted such that the maximum parallax is in the permissible range even when an imaging subject approaches to immediately in front of an image capture device for capturing the video image.
8. The parallax adjustment method for a 3D image reproduction apparatus of claim 5, wherein, in parallax adjustment, horizontal direction display positions of a right eye image and a left eye image of each of the frames are shifted such that the maximum parallax is within the permissible range.
9. A non-transitory computer-readable storage medium that stores a parallax adjustment program that causes a computer to function as:
an acquisition section that acquires video image data configured from a right eye image and a left eye image for displaying a 3D image, image capture shortest distance data representing an image capture shortest distance during image capture of the video image data, image capture data for computing distance, and parallax data representing a setting parallax that is set for the right eye image and the left eye image;
a computation section that detects a predetermined main imaging subject in each frame of the video image data, that computes a main imaging subject parallax for each of the frames based on the detected main imaging subject, and that employs the image capture data and the setting parallax to compute a relationship between the main imaging subject parallax and a main imaging subject distance; and
an adjustment section that, when the image capture shortest distance data has been acquired by the acquisition section, adjusts the setting parallax acquired by the acquisition section such that a maximum parallax of the main imaging subject is within a predetermined permissible range when image capture was at the image capture shortest distance, using the relationship between the main imaging subject parallax and the main imaging subject distance that has been computed by the computation section.
10. An image capture device equipped with the 3D image reproduction apparatus of claim 1.