“…Could it be that different disorders give rise to different glass transition temperatures? If we are dealing with structural (SG) and orientational glasses (OG), the dynamic disorder is governed by the so-called α-dielectric relaxation, which embeds the different disorders present in the vitrified phase and, therefore, there is just one glass transition temperature [ 3 , 4 , 5 , 6 , 7 ]. The main dynamic disorders represented by the α-relaxation are translational and orientational in the SG and orientational in the OG.…”
In the present work, the nematic glassy state of the non-symmetric LC dimer α-(4-cyanobiphenyl-4′-yloxy)-ω-(1-pyrenimine-benzylidene-4′-oxy) undecane is studied by means of calorimetric and dielectric measurements. The most striking result of the work is the presence of two different glass transition temperatures: one due to the freezing of the flip-flop motions of the bulkier unit of the dimer and the other, at a lower temperature, related to the freezing of the flip-flop and precessional motions of the cyanobiphenyl unit. This result shows the fact that glass transition is the consequence of the freezing of one or more coupled dynamic disorders and not of the disordered phase itself. In order to avoid crystallization when the bulk sample is cooled down, the LC dimer has been confined via the dispersion of γ-alumina nanoparticles, in several concentrations.
“…Could it be that different disorders give rise to different glass transition temperatures? If we are dealing with structural (SG) and orientational glasses (OG), the dynamic disorder is governed by the so-called α-dielectric relaxation, which embeds the different disorders present in the vitrified phase and, therefore, there is just one glass transition temperature [ 3 , 4 , 5 , 6 , 7 ]. The main dynamic disorders represented by the α-relaxation are translational and orientational in the SG and orientational in the OG.…”
In the present work, the nematic glassy state of the non-symmetric LC dimer α-(4-cyanobiphenyl-4′-yloxy)-ω-(1-pyrenimine-benzylidene-4′-oxy) undecane is studied by means of calorimetric and dielectric measurements. The most striking result of the work is the presence of two different glass transition temperatures: one due to the freezing of the flip-flop motions of the bulkier unit of the dimer and the other, at a lower temperature, related to the freezing of the flip-flop and precessional motions of the cyanobiphenyl unit. This result shows the fact that glass transition is the consequence of the freezing of one or more coupled dynamic disorders and not of the disordered phase itself. In order to avoid crystallization when the bulk sample is cooled down, the LC dimer has been confined via the dispersion of γ-alumina nanoparticles, in several concentrations.
“…In our case, we obtained 119 for poly2‐4 and 151 for poly2‐6. The lower limit of m is assigned to 16, the strongest materials 35, 36. On the other hand, the most fragile glass‐forming materials have values of m up to 200 or even more.…”
“…As for cC7‐ol, in addition to the α ‐relaxation, it only shows one secondary process ascribed to the axial and equatorial orientations of the –OH group and, by analogy with cC8‐ol is called γ ‐relaxation 11. It should be mentioned that some authors argued the existence of a β ‐relaxation also for cC7‐ol 22.…”
Low‐molecular weight cyclic alcohols as cycloheptanol (C7H14O, hereinafter referred to as cC7‐ol) and cyclooctanol (C8H16O, cC8‐ol) are prototypical materials displaying OD phases which, under fast cooling give rise to orientational glasses (OG). In addition to the ubiquitous α‐relaxation of canonical glasses, several secondary relaxations appear for the mentioned systems (β and γ for cC8‐ol and β for cC7‐ol). The intramolecular character of these secondary relaxations for these materials as well as their mixed crystals was highlighted at temperatures close but above the glass transition. For lower temperatures the low values of dielectric strength makes difficult to account for the relaxation times obtained from the permittivity losses and, thus in this work we present a data analysis based on the Kramers–Kronig relations which connect the real and imaginary parts of dielectric permittivity and shows up a new method to make evident the existence of such secondary relaxations as well as to avoid phenomenological equations for determining the relaxation time.
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