Cationic quaternary ammonium gemini surfactants CnH(2n+1)(CH3)(2)N+CH2CHCHCH2(CH3)(2)N(+)C(n)H(2)n(+1)2Br(-)(CnC4Cn, n = 12, 8, 6) with alkyl spacers, CnH2n+1 (CH3)(2-) N+CH2 C H O H C H O H C H-2 (CH3)(2)N(+)C(n)H(2n+1)2Br(-)(CnC4(OH)(2)C-n, n = 12, 8, 6, 4) with two hydroxyl groups in alkyl spacers, and cationic ammonium single-chain surfactants CnH2n+1(CH3)(2)N+Br- (C(n)TAB, n = 12, 8, 6) have been chosen to fabricate oppositely charged surfactant mixtures with anionic sulfonate gemini surfactant C12H25N(CH2CH2CH2SO3-)CH2-CH2CH2(CH3)(2)N(CH2CH2CH2SO3-)C(12)H(25)2Na (C12C3C12(SO3)(2)). Surface tension, electrical conductivity, and isothermal titration microcalorirnetry (ITC) were used to study their surface properties, aggregation behaviors, and intermolecular interactions. The mixtures of C12C3C12(SO3)(2)/CnC4(OH)(2)C-n (n = 12, 8) and C12C3C12(SO3)(2)/C12C4C12 show anomalous larger critical micelle concentration (CMC) than C12C3C12(SO3)(2), while the mixtures of C12C3C12(SO3)(2)/CnC4(OH)(2)C-n (n = 6, 4), C12C3C12(SO3)(2)/CnC4(OH)(2)C-n (n = 6, 4), and C12C3C12(SO3)(2)/ C(n)TAB (n = 12, 8, 6) exhibit much lower CMC than C12C3C12(SO3)(2). The results indicate that strong hydrophobic interactions between the alkyl chains assisted by strong electrostatic attractions between the headgroups and hydrogen bonds between the spacers lead to the formation of less surface active premicellar aggregates in bulk solution, resulting in the increase of CMC. If these interactions are weakened or inhibited, less surface active premicellar aggregates are no longer formed in the mixtures, and thus the CMC values are reduced. The work reveals that the combination of two surfactants with great self-assembling ability separately may have strong intermolecular binding interactions; however, their mixtures do not always generate superior synergism properties. Only moderate intermolecular interaction can generate the strongest synergism in CMC reduction.