1994
DOI: 10.1021/cm00044a037
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Optical, Calorimetric, and Mass Spectroscopic Study of Nonthermochromic Crystalline Forms of the Polydiacetylene Bis(ethylurethane)-5,7-Dodecadiyne-1,12-diol (ETCD)

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Cited by 17 publications
(15 citation statements)
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“…Association between end groups can be based on a variety of secondary interactions, such as van der Waals, hydrophobic, ionic interactions, or hydrogen bonding. [4] In these polymers, relatively weak association in combination with crystallization leads to physical crosslinks, which result in materials with improved properties. [1] In these materials a reversible network is formed by clustering of the end groups.…”
Section: Methodsmentioning
confidence: 99%
“…Association between end groups can be based on a variety of secondary interactions, such as van der Waals, hydrophobic, ionic interactions, or hydrogen bonding. [4] In these polymers, relatively weak association in combination with crystallization leads to physical crosslinks, which result in materials with improved properties. [1] In these materials a reversible network is formed by clustering of the end groups.…”
Section: Methodsmentioning
confidence: 99%
“…[48] Exposure of single crystals of the PDA derived from bis(ethylurethane)-5,7-dodecadiybe-1,12-diol (ETDC) to boiling chlorobenzene results in the significant blue shift in the near-normal incidence reflection spectra. [51] The color change of the crystals is attributed to the loss of the unreacted monomers and oligomers, which results in an increase in the lattice volume. Thus, reduction of the restriction of a mechanical strain imposed on the polymer sidechains may induce partial distortion of the conjugated p-orbitals, leading to the blue-shift in the reflection spectra.…”
Section: Feature Articlementioning
confidence: 99%
“…Third, PDAs are readily prepared in aqueous solution in the form of nanostructured liposomes, vesicles and wires, properties that enable them to be employed as matrices for biosensing. Finally, nanostructured PDAs undergo a blue-to-red color change in response to heat (thermochromism), [23,46,47] organic solvents (solvatochromism), [48][49][50][51][52] mechanical stress (mechanochromism), [53][54][55][56] and ligandreceptor interactions (affinochromism). [57][58][59][60][61][62][63][64][65][66][67][68][69] The majority of PDA-based chemosensors, reported thus far, function in an irreversible fashion.…”
Section: Introductionmentioning
confidence: 99%
“…Unlike other conjugated polymers, PDAs are uniquely prepared by UV or γ ‐irradiation of molecularly assembled diacetylene monomers without employing additional catalysts or initiators 1–22. Undoubtedly, the most attractive property of PDAs is their brilliant blue‐to‐red color transition, which occurs with environmental perturbations such as heat (thermochromism),23, 24 mechanical stress (mechanochromism),25–28 organic solvents (solvatochromism),29–33 and ligand–receptor interactions (affinochromism) 34–45. These stress‐induced responses that generate a simultaneous fluorescence signal have efficiently been applied to design of bio‐ and chemosensors,34–45 molecular switches,46, 47 photonic materials,48 and information displays 49.…”
Section: Introductionmentioning
confidence: 99%