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We show, with the help of polarized neutrons, that the cubic magnets Fe1-xCoxSi with Dzyaloshinskii-Moriya interaction can be switched between left (for x=0.1, 0.15) and right (for x=0.2, 0.25, 0.3, 0.5) chiral states of the spin helix. The absolute structure was evaluated using x-ray diffraction. The crystals are shown to be enantiopure and the structural chirality changes from right handed for x<0.2 to left handed for x>0.2. These compounds are compared with the etalon sample of MnSi which is identified as having the left-handed chirality both in the magnetic and crystallographic sense.

Magnetic susceptibility measurements have shown that the compounds Mn(1-x)Fe(x)Ge are magnetically ordered through the whole range of concentrations x = [0.0,1.0]. Small-angle neutron scattering reveals the helical nature of the spin structure with a wave vector, which changes from its maximum (|k| = 2.3 nm(-1)) for pure MnGe, through its minimum (|k| → 0) at x(c) ≈ 0.75, to the value of |k| = 0.09 nm(-1) for pure FeGe. The macroscopic magnetic measurements confirm the ferromagnetic nature of the compound with x = x(c). The observed transformation of the helix structure to the ferromagnet at x = x(c) is explained by different signs of chirality for the compounds with x > x(c) and x

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