2011
DOI: 10.1002/cjoc.201190078
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Syntheses, Optical Properties and Photoactivated Insecticidal Activities of Cyclic Arylethynylsilanes

Abstract: Syntheses and optical properties of cyclic arylethynylsilanes containing one or two trialkyne pockets were described. Optical properties such as UV-vis spectra, photoluminescence and quantum yield based on these conjugated structural features were compared with each other. The photoactivated insecticidal activities against the 4th-instar larvae of Aedes albopictus (Skuse) were evaluated.

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Cited by 6 publications
(3 citation statements)
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“…15 It is highly possible to tailor desirable optoelectronic properties of such molecules by manipulation of the parent chromophore, which includes conjugation length control and the introduction of electron donating or withdrawing groups into the primary chemical structure. 16,17 In this work, to develop red phosphors with advantageous properties, a series of europium(III)-b-diketonate complexes based on diphenylethyne with different substituents were synthesized. Their photophysical properties, thermal stability, energy-transfer mechanism and structure-property relationships were investigated.…”
Section: Introductionmentioning
confidence: 99%
“…15 It is highly possible to tailor desirable optoelectronic properties of such molecules by manipulation of the parent chromophore, which includes conjugation length control and the introduction of electron donating or withdrawing groups into the primary chemical structure. 16,17 In this work, to develop red phosphors with advantageous properties, a series of europium(III)-b-diketonate complexes based on diphenylethyne with different substituents were synthesized. Their photophysical properties, thermal stability, energy-transfer mechanism and structure-property relationships were investigated.…”
Section: Introductionmentioning
confidence: 99%
“…This dual functionalities extend their potential applications to nonlinear optical materials, liquid crystal materials, and molecular devices [3] . Interestingly, it has been recently reported that this class of diynes also exhibits photoactivatable insecticidal properties and is a key structure for a potential class of highly efficient and low‐toxic ecological photoactivatable pesticides [4] . Diyne's pivotal role is evident in the synthesis of diverse alkynes types, the construction of macrocyclic alkynes, natural product synthesis and supramolecular fields [5] .…”
Section: Introductionmentioning
confidence: 98%
“…[3] Interestingly, it has been recently reported that this class of diynes also exhibits photoactivatable insecticidal properties and is a key structure for a potential class of highly efficient and low-toxic ecological photoactivatable pesticides. [4] Diyne's pivotal role is evident in the synthesis of diverse alkynes types, the construction of macrocyclic alkynes, natural product synthesis and supramolecular fields. [5] In summary, conjugated diynes exhibit exceptional properties that make them invaluable in pharmaceuticals, materials, pesticides, and fine synthesis, all thanks to their distinctive structures.…”
Section: Introductionmentioning
confidence: 99%