Metalloenzyme inhibitor compounds

A composition comprising a compound of Formula I, or salt thereof, and an agriculturally acceptable carrier;

• wherein MBG is optionally substituted tetrazolyl, optionally substituted triazolyl, optionally substituted oxazolyl, optionally substituted pyrimidinyl, optionally substituted thiazolyl, or optionally substituted pyrazolyl;
• R1 is H, halo, alkyl, or haloalkyl;
• R2 is H, halo, alkyl, or haloalkyl:
• R3 is independently H, alkyl, alkenyl, cycloalkyl, heteroaryl, hydroxyalkyl, cyano, haloalkyl, halo, —C(O)phenyl, —CH(OH)(aryl), —CH(aryl), —CH2(heteroaryl), —CF(aryl), —CF2(heteroaryl), —CH2O(aryl), —CH2O(heteroaryl), —CH2S(O)X(aryl), and cyclic amino, wherein each of the alkyl, alkenyl, cycloalkyl, heteroaryl, hydroxyalkyl, haloalkyl, —C(O)phenyl, —CH(OH)(aryl), —CH2(aryl), —CH2(heteroaryl), —CF2(aryl), CF2(heteroaryl), —CH2O(aryl), —CH2O(heteroaryl), —CH2S(O)x(aryl), and cyclic amino may be optionally substituted with 1, 2 or 3 independent R7;
• R4 is aryl, heteroaryl, or cycloalkyl, each optionally substituted with 0, 1, 2 or 3 independent R8;
• R5 is independently H, halo, alkyl, alkoxy, cyano, haloalkyl, haloalkoxy, halothioalkyl, thioalkyl, SF3, SF6, SCN, SO2R11, cycloalkyl, —C(O)alkyl, —C(O)OH, —C(O)Oalkyl;
• R6 is independently H, halo, alkyl, alkoxy, cyano, haloalkyl, haloalkoxy, halothioalkyl, thioalkyl, SF3, SF6, SCN, SO2R11, cycloalkyl, —C(O)alkyl, —C(O)OH, —C(O)Oalkyl;
• each R7 is independently cyano, cycloalkyl, haloalkyl, hydroxy, alkoxy, aryl, aryloxy, heteroaryloxy, halo, haloalkoxy, —C(O)alkyl, —C(O)OH, —C(O)Oalkyl;
• each R8 is independently cyano, haloalkyl, hydroxy, alkoxy, halo, or haloalkoxy;
• R9 is H, halo, or haloalkyl;
• R10 is H, alkyl, —Si(R12)3, —P(O)(OH)2, —CH—O—P(O)(OH)2, or —C(O)alkyl optionally substituted with amino;
• R11 is independently alkyl, aryl, substituted aryl, heteroaryl or substituted heteroaryl;
• R12 is independently alkyl or aryl;
• and
• x is independently 0, 1, or 2.