3 research outputs found
Crystals and Aggregates of a Molecular Tetrarotor with Multiple Trityl Embraces Derived from Tetraphenyladamantane
Samples of tetrakis-1,3,5,7-(4′-(3″,3″,3″-triphenylpropynyl)-phenylene)Âadamantane
and its trityl-deuterated isotopologue were synthesized and their
crystallization and packing properties were analyzed within the context
of formation of 4- or 6-fold phenyl embraces. The tetrahedral shape
of these molecules with four propeller-like triphenylmethyl moieties
generates several edge-to-face intermolecular interactions in the
solid state that result in the formation of infinite chains of molecules
that are tightly interlocked. The formation of analogous edge-to-face
intermolecular interactions leading to aggregation in solution was
also suggested by NMR experiments carried out in different solvents
as a function of concentration. The formation of interdigitated chains
was also manifested in fibrils and thin needles, which were documented
by scanning electron microscopy (SEM). Single crystal X-ray diffraction
studies revealed the presence of multiple 4-fold phenyl embraces and
edge-to-face interactions as the leading motifs behind the formation
of tightly interlocked molecular chains
Crystals and Aggregates of a Molecular Tetrarotor with Multiple Trityl Embraces Derived from Tetraphenyladamantane
Samples of tetrakis-1,3,5,7-(4′-(3″,3″,3″-triphenylpropynyl)-phenylene)Âadamantane
and its trityl-deuterated isotopologue were synthesized and their
crystallization and packing properties were analyzed within the context
of formation of 4- or 6-fold phenyl embraces. The tetrahedral shape
of these molecules with four propeller-like triphenylmethyl moieties
generates several edge-to-face intermolecular interactions in the
solid state that result in the formation of infinite chains of molecules
that are tightly interlocked. The formation of analogous edge-to-face
intermolecular interactions leading to aggregation in solution was
also suggested by NMR experiments carried out in different solvents
as a function of concentration. The formation of interdigitated chains
was also manifested in fibrils and thin needles, which were documented
by scanning electron microscopy (SEM). Single crystal X-ray diffraction
studies revealed the presence of multiple 4-fold phenyl embraces and
edge-to-face interactions as the leading motifs behind the formation
of tightly interlocked molecular chains
Photoinduced and Thermal Denitrogenation of Bulky Triazoline Crystals: Insights into Solid-to-Solid Transformation
The
photoinduced and thermal denitrogenation of crystalline triazolines
with bulky substituents leads to the quantitative formation of aziridines
in clean solid-to-solid reactions despite very large structural changes
in the transition from reactant to product. Analysis of the reaction
progress by powder X-ray diffraction, solid-state <sup>13</sup>C CPMAS
NMR, solid-state FTIR spectroscopy, and thermal analysis has revealed
that solid-to-solid reactions proceed either through metastable phases
susceptible to amorphization or by mechanisms that involve a reconstructive
phase transition that culminates in the formation of the stable phase
of the product. While the key for a solid-to-solid transformation
is that the reaction occurs below the eutectic temperature of the
reactant and product two-component system, experimental evidence suggests
that those reactions will undergo a reconstructive phase transition
when they take place above the glass transition temperature