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We search for a Gardner transition in glassy glycerol, a standard molecular glass, measuring the third harmonics cubic susceptibility χ_{3}^{(3)} from slightly below the usual glass transition temperature down to 10 K. According to the mean-field picture, if local motion within the glass were becoming highly correlated due to the emergence of a Gardner phase then χ_{3}^{(3)}, which is analogous to the dynamical spin-glass susceptibility, should increase and diverge at the Gardner transition temperature T_{G}. We find instead that upon cooling |χ_{3}^{(3)}| decreases by several orders of magnitude and becomes roughly constant in the regime 100-10  K. We rationalize our findings by assuming that the low temperature physics is described by localized excitations weakly interacting via a spin-glass dipolar pairwise interaction in a random magnetic field. Our quantitative estimations show that the spin-glass interaction is twenty to fifty times smaller than the local random field contribution, thus rationalizing the absence of the spin-glass Gardner phase. This hints at the fact that a Gardner phase may be suppressed in standard molecular glasses, but it also suggests ways to favor its existence in other amorphous solids and by changing the preparation protocol.

The volborthite compound is one of the very few realizations of S=1/2 quantum spins on a highly frustrated kagomé-like lattice. Low-T SQUID measurements reveal a broad magnetic transition below 2 K which is further confirmed by a peak in the 51V nuclear spin relaxation rate (1/T1) at 1.4 K +/- 0.2 K. Through 51V NMR, the ground state (GS) appears to be a mixture of different spin configurations, among which 20% corresponds to a well defined short-range order, possibly of the sqrt(3) x sqrt(3) type. While the freezing involves all the Cu2+ spins, only 40% of the copper moment is actually frozen which suggests that quantum fluctuations strongly renormalize the GS.