Crystallized diacetylenic indicator compounds and methods of preparing the compounds
View Patent ↗Crystallized diacetylenic compounds having certain crystallographic and other characteristics; diacetylenic compounds and mixtures crystallized from diacetylenic solutions; methods of preparing and identifying solvent systems for dissolving diacetylenic compounds; diacetylenic solutions; methods of recrystallizing diacetylenic compounds; crystals of 2,4-hexadiyn-1,6-bis(alkylurea) compounds; and ambient condition indicators and time-temperature condition indicators comprising crystallized diacetylenic compounds.
1. A crystallized diacetylenic compound capable of polymerizing in the solid state to provide an irreversible appearance change in an environmental condition indicator, the crystallized diacetylenic compound being symmetrically substituted and having the structural formula:
R′NHCONH—R—C≡C—C≡C—R—NHCONHR′
wherein R is methylene, ethylene, propylene or butylene, R′ is ethyl or propyl, the crystallized diacetylenic compound having a crystal structure wherein the crystallized diacetylenic compound molecules have a center-to-center separation, referring to the geometric centers of diacetylene units in adjacent molecules, of less than 4.7 Å, the center-to-center separation being in a direction wherein solid-state polymerization can occur.
2. A crystallized diacetylenic compound according to claim 1 wherein the center-to-center separation corresponds to a unit cell repeat distance of the crystallized diacetylenic compound.
3. A crystallized diacetylenic compound according to claim 1 comprising two hydrogen bonds for each NHCONH urea group, each one of the two hydrogen bonds extending between one of the two NH groups in a urea group in one polymerizable diacetylenic molecule and a C═ 0 group in an adjacent polymerizable diacetylenic molecule.
4. A crystallized diacetylenic compound according to claim 1 having a triclinic crystal structure including a center of symmetry wherein no axes or planes of symmetry exist.
5. A crystallized diacetylenic compound according to claim 1 having a monoclinic crystal structure.
6. A crystallized diacetylenic compound according to claim 1 having a purity of at least about 99 percent by weight.
7. A crystallized diacetylenic compound according to claim 1 comprising at least one non-acetylenic compound in the crystal phase.
8. A crystallized diacetylenic compound according to claim 1 comprising not more than about 3 percent by weight of the polymerized diacetylenic compound, based upon the weight of the diacetylenic compound and the polymer.
9. An ambient condition indicator comprising a crystallized diacetylenic compound according to claim 1 .
10. The crystallized diacetylenic compound of claim 1 wherein the 2,4-hexadiyn-1,6-bis(alkylurea) compound is 2,4-hexadiyn-1,6-bis(ethylurea).
11. The crystallized diacetylenic compound of claim 1 wherein the 2,4-hexadiyn-1,6-bis(alkylurea) compound is 2,4-hexadiyn-1,6-bis(propylurea).
12. The crystallized diacetylenic compound of claim 1 having a X-ray diffraction pattern that lacks high intensity peaks at high 2θ diffraction angles in the range of from about 19 degrees to about 24 degrees.
13. The crystallized diacetylenic compound of claim 12 , comprising a first high intensity peak at a 20 diffraction angles in the range of from about 4 degrees to about 6 degrees and a second high intensity peak at a 20 diffraction angle in the range of from about 8 degrees to about 12 degrees.
14. The crystallized diacetylenic compound of claim 13 wherein the crystal exhibits a d spacing corresponding with the first high intensity peak being half the value of the d spacing corresponding with the second high intensity peak.
15. The crystallized diacetylenic compound of claim 14 wherein the first high intensity peak and the second highest peak have a harmonic relationship one peak to the other peak.
16. An ambient condition indicator comprising crystals of a 2,4-hexadiyn-1,6-bis(alkylurea) compound according to claim 10 .