Pesticidally active pyrazole derivatives

A compound of formula (I)

• wherein
• R1 is selected from H, C1-C6-alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C7 cycloalkyl, C3-C7 cycloalkyl-C1-C3-alkyl, C1-C6-alkylcarbonyl, C1-C6-alkoxycarbonyl, aryl(C0-C3)-alkyl and heteroaryl(C0-C3)-alkyl, wherein each of C1-C6-alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C7 cycloalkyl, C3-C7 cycloalkyl-C1-C3-alkyl, C1-C6-alkylcarbonyl, C1-C6-alkoxycarbonyl, aryl(C0-C3)-alkyl and heteroaryl(C0-C3)-alkyl is unsubstituted or substituted with 1 to 7 substituents independently selected from halogen, cyano, C1-C6-alkoxy and C1-C6-alkoxycarbonyl;
• Q is selected from H, hydroxy, —C(═O)H, C1-C6-alkyl, C1-C6-alkoxy, C2-C6 alkenyl, C2-C6 alkinyl, C3-C7 cycloalkyl, C3-C7 heterocycloalkyl, C3-C7 cycloalkyl-C1-C3-alkyl, C1-C3-alkyl-C3-C7 cycloalkyl, aryl(C0-C3)-alkyl, heteroaryl(C0-C3)-alkyl, N—C1-C6-alkylamino, N—C1-C6-alkylcarbonylamino and N,N-di (C1-C6-alkyl)amino, wherein each of C1-C6-alkyl, C1-C6-alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, C3-C7 cycloalkyl, C3-C7 heterocycloalkyl, C3-C7 cycloalkyl-C1-C3-alkyl, C1-C3-alkyl-C3-C7 cycloalkyl, aryl(C0-C3)-alkyl, heteroaryl(C0-C3)-alkyl, N—C1-C6-alkylamino, N—C1-C6-alkylcarbonylamino and N,N-di (C1-C6-alkyl)amino is unsubstituted or substituted with 1 to 7 substituents independently selected from halogen, hydroxyl, nitro, amino, cyano, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkoxycarbonyl, —C(═O)OH, C1-C6-alkylcarbamoyl, —C(═O)NH2, —C(═S)NH2, C3-C6-cycloalkylcarbamoyl and phenyl;
• W is O or S;
• L is selected from
• wherein
• indicates the bond to the group
• T is a 5-membered heteroaryl of formula
• wherein
• indicates the bond to the group
• and * indicates the bond to the pyrazole ring;
• D1 is selected from CR9a, N, NR9b, O and S;
• D2 is selected from CR10a, N, NR10b, O and S;
• D3 is C or N;
• D4 is selected from CR11a, N, NR11b, O and S;
• D5 is C or N;
• with the proviso that at least one of D1, D2, D3, D4 and D5 is selected from N, O and S, that no more than one of D1, D2 and D4 is O or S, and that no more than three of D1, D2, D3, D4 and D5 are N and that D5 is C when L is L1, L6, L10, L11, L38, L39 or L43;
• R6a, R7a, R8a, R9a, R10a and R11a are independently selected from H, halogen, cyano, nitro, amino, C1-C6-alkyl, C1-C6-alkoxy, C3-C7 cycloalkyl, C1-C6-alkylcarbonyl, C1-C6-alkylsulfanyl, C1-C6-alkylsulfinyl and C1-C6-alkylsulfonyl, wherein each of C1-C6-alkyl, C1-C6-alkoxy, C3-C7 cycloalkyl, C1-C6-alkylcarbonyl, C1-C6-alkylsulfanyl, C1-C6-alkylsulfinyl and C1-C6-alkylsulfonyl is unsubstituted or substituted with 1 to 7 halogen;
• R6b, R7b, R8b, R9b, R10b and R11b are independently selected from H and C1-C6-alkyl, wherein C1-C6-alkyl is unsubstituted or substituted with 1 to 7 halogen;
• U is selected from —O—, —S—, —SO—, —SO2— and —NR100—;
• R100 is selected from H, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy, C1-C6-alkylcarbonyl, C1-C6-alkoxycarbonyl and C3-C6-cycloalkyl, wherein each of C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy and C3-C6-cycloalkyl is unsubstituted or substituted with 1 to 13 substituents independently selected from halogen;
• Z1 is selected from C1-C10-alkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkoxy-C1-C6-alkyl, C2-C10-alkenyl, C2-C10-alkynyl, —(C0-C6-alkyl)-C3-C7 heterocycloalkyl, —(C0-C6-alkyl)-C3-C6-cycloalkyl and C1-C10-alkylsulfonyl, wherein each of C1-C10-alkyl, C1-C6-alkoxy-C1-C6-alkyl, C1-C6-alkoxy-C1-C6-alkoxy-C1-C6-alkyl, C2-C10-alkenyl, C2-C10-alkynyl, —(C0-C6-alkyl)-C3-C7 heterocycloalkyl, —(C0-C6-alkyl)-C3-C6-cycloalkyl and C1-C10-alkylsulfonyl is unsubstituted or substituted with 1 to 20 substituents independently selected from halogen, hydroxy, nitro, amino, cyano, C1-C6-alkoxy, C1-C6-alkoxycarbonyl, hydroxycarbonyl, C1-C6-alkylcarbamoyl, C3-C6-cycloalkylcarbamoyl and phenyl;
• Z2 is selected from H, halogen, cyano, nitro, amino, C1-C6-alkyl, C1-C6-alkylcarbonyl, C1-C6-alkylsulfanyl, C1-C6-alkylsulfinyl and C1-C6-alkylsulfonyl, wherein each of C1-C6-alkyl, C1-C6-alkylcarbonyl, C1-C6-alkylsulfanyl, C1-C6-alkylsulfinyl and C1-C6-alkylsulfonyl is unsubstituted or substituted with 1 to 5 substituents independently selected from halogen, hydroxy, nitro, amino, cyano, C1-C6-alkoxy, C1-C6-alkoxycarbonyl, hydroxycarbonyl, C1-C6-alkylcarbamoyl, C3-C6-cycloalkylcarbamoyl and phenyl;
• Z3 is selected from H, C1-C6-alkyl, C1-C6-cycloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, aryl and heteroaryl, wherein each of C1-C6-alkyl, C1-C6-cycloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, aryl and heteroaryl, is unsubstituted or substituted with 1 to 7 substituents independently selected from halogen, hydroxy, nitro, amino, cyano, C1-C6-alkoxy, C1-C6-alkoxycarbonyl, —C(═O)OH, C1-C6-alkylcarbamoyl, C3-C6-cycloalkylcarbamoyl and phenyl;
• with the proviso that when L is L46 and Z1 is C1-C6-alkyl, U is not —O—;
• or an agrochemically acceptable salt or N-oxide thereof.