Abstract:Rigid cyclic molecules are of great interest due to their intriguing structures and unique properties. Here, we report the facile synthesis of gem-linked cyclic tetraphenylethylenes and cyclic hexaphenylethylenes, namely [n]CTPEs...
“…[8] In 2022, we successfully synthesized [n]gem-link cyclic tetraphenylethylenes ([n]g-CTPEs) (Figure 1c) and [n] gem-link cyclic hexaphenylethylenes ([n]g-CHPEs). [9] We found that the strain energy of [2]g-CTPE reached an impressive 256.06 • kJ mol À 1 and [2]g-CTPE emits intense blue light in both solution and aggregated states, exhibiting a dual-state luminescence phenomenon. As a continuous part of this research, we decided to synthesize the cis-connected cyclotetraphenylethylenes, namely [n]c-CTPEs (Figure 1d), and make comparisons on the structures and fluorescence properties of the cis-connected cyclic tetraphenylethylenes with the gem-linked tetraphenylethylene analogues.…”
Section: Introductionmentioning
confidence: 91%
“…We are interested in the synthesis and properties of highly strained molecules [8] . In 2022, we successfully synthesized [n] gem ‐link cyclic tetraphenylethylenes ( [n] g ‐CTPEs ) (Figure 1c) and [n] gem ‐link cyclic hexaphenylethylenes ( [n] g ‐CHPEs ) [9] . We found that the strain energy of [ 2] g ‐CTPE reached an impressive 256.06 ⋅ kJ mol −1 and [2] g ‐CTPE emits intense blue light in both solution and aggregated states, exhibiting a dual‐state luminescence phenomenon.…”
cis‐Linked cyclotetraphenylene dimer [2]c‐CTPE and trimer [3]c‐CTPE were synthesized via Pt‐mediated cyclization of cis‐diboronated tetraphenylethene. The structure of [2]c‐CTPE has been confirmed by single crystal X‐ray diffraction. The strain energy of [2]c‐CTPE and [3]c‐CTPE was calculated to be 86.28·kJ mol‐1 and 9.23 kJ·mol‐1, respectively. [2]c‐CTPE and [3]c‐CTPE are typical AIEgens and show mechanofluorochromic properties. The comparisons of cis‐linked cyclotetraphenylenes with gem‐linked cyclotetraphenylenes were also discussed.
“…[8] In 2022, we successfully synthesized [n]gem-link cyclic tetraphenylethylenes ([n]g-CTPEs) (Figure 1c) and [n] gem-link cyclic hexaphenylethylenes ([n]g-CHPEs). [9] We found that the strain energy of [2]g-CTPE reached an impressive 256.06 • kJ mol À 1 and [2]g-CTPE emits intense blue light in both solution and aggregated states, exhibiting a dual-state luminescence phenomenon. As a continuous part of this research, we decided to synthesize the cis-connected cyclotetraphenylethylenes, namely [n]c-CTPEs (Figure 1d), and make comparisons on the structures and fluorescence properties of the cis-connected cyclic tetraphenylethylenes with the gem-linked tetraphenylethylene analogues.…”
Section: Introductionmentioning
confidence: 91%
“…We are interested in the synthesis and properties of highly strained molecules [8] . In 2022, we successfully synthesized [n] gem ‐link cyclic tetraphenylethylenes ( [n] g ‐CTPEs ) (Figure 1c) and [n] gem ‐link cyclic hexaphenylethylenes ( [n] g ‐CHPEs ) [9] . We found that the strain energy of [ 2] g ‐CTPE reached an impressive 256.06 ⋅ kJ mol −1 and [2] g ‐CTPE emits intense blue light in both solution and aggregated states, exhibiting a dual‐state luminescence phenomenon.…”
cis‐Linked cyclotetraphenylene dimer [2]c‐CTPE and trimer [3]c‐CTPE were synthesized via Pt‐mediated cyclization of cis‐diboronated tetraphenylethene. The structure of [2]c‐CTPE has been confirmed by single crystal X‐ray diffraction. The strain energy of [2]c‐CTPE and [3]c‐CTPE was calculated to be 86.28·kJ mol‐1 and 9.23 kJ·mol‐1, respectively. [2]c‐CTPE and [3]c‐CTPE are typical AIEgens and show mechanofluorochromic properties. The comparisons of cis‐linked cyclotetraphenylenes with gem‐linked cyclotetraphenylenes were also discussed.
“…In 2022, Jiang and colleagues reported a series of tetraphenylethylene (TPE) containing macrocycles 49 ( i.e. , [ n ]CTPE 49 and [ n ]CHPE 50 ) (Fig.…”
Section: Carbon-rich Macrocycles As Potential Optical Materialsmentioning
Carbon-rich macrocycles and carbon nanoribbons are considered as the combination of carbon rich molecular materials and supramolecular macrocycle hosts. They can act as unique optical material candidate choices with free...
“…[20][21][22] Tetraphenylethylene (TPE) is a star molecule of AIE materials, widely used due to its simple synthesis, modification, and unusual luminescence. [23][24][25][26][27][28][29][30][31][32][33][34][35][36] A series of eightshaped double macrocycles can be formed by connecting the benzene rings of TPE in pairs (Scheme 1). These structures have received great attention, leading to a series of studies on the AIE mechanism, ion recognition, and multicolor luminescence.…”
In the past few decades, macrocycles with different structures and functions have played a crucial role in supramolecular chemistry. Due to its symmetrical structure, simple synthesis process, good stability, and...
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