A carborane-perylene diimide derivative and its synthesis method, sensor array based on it, its preparation method and application
A technology of perylene diimide and sensing array, which is applied in the field of small molecule fluorescent sensing thin film materials, can solve the problems of increasing the difficulty of the preparation process, large differences in excitation and emission characteristics, and complex synthesis methods of fluorescent components, and achieves a practical High performance, eliminate interference, and ensure the effect of simplicity
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Embodiment 1
[0069] Synthesis of carborane-perylene diimide derivatives (in this example, n=9)
[0070] Wherein the raw material selects p-iodoaniline, p-ethynyl aniline, and the alkyl ketone selects 12-tritricone;
[0071] (1) Synthesis of compound 1
[0072] Take by weighing 2.19g p-iodoaniline, 0.58g Pd(PPh 3 ) 4 , 0.095g CuI and 1.17g p-ethynylaniline were placed in a 100mL two-necked bottle. Under nitrogen protection, 10 mL of triethylamine and 40 mL of tetrahydrofuran were sequentially added to the reaction system, heated to 70° C., stirred for 12 hours, cooled to room temperature, and spin-dried. A brown solid was obtained by column chromatography using dichloromethane:petroleum ether (1:1) as the eluent. The resulting solid was dried under vacuum at 50°C. Its reaction equation is as follows:
[0073]
[0074] (2) Synthesis of compound 2
[0075] Weigh 3.39g of 12-docotriconone and 1.38g of hydroxylamine hydrochloride in a 100mL single-necked bottle, add 10mL of pyridine a...
Embodiment 2
[0091] Synthesis of carborane-perylene diimide derivatives (n=5 in this embodiment)
[0092] Wherein the raw material selects p-iodoaniline, p-ethynyl aniline, and the alkyl ketone selects 8-pentadecanone;
[0093] (1) Synthesis of compound 1
[0094] Take by weighing 2.19g p-iodoaniline, 0.58g Pd(PPh 3 ) 4 , 0.095g CuI and 1.17g p-ethynylaniline were placed in a 100mL two-necked bottle. Under nitrogen protection, 10 mL of triethylamine and 40 mL of tetrahydrofuran were sequentially added to the reaction system, heated to 70° C., stirred for 12 hours, cooled to room temperature, and spin-dried. A brown solid was obtained by column chromatography using dichloromethane:petroleum ether (1:1) as the eluent. The resulting solid was dried under vacuum at 50°C. Its reaction equation is as follows:
[0095]
[0096] (2) Synthesis of compound 2
[0097] Weigh 2.26g of 8-pentadecanone and 1.38g of hydroxylamine hydrochloride in a 100mL single-necked bottle, add 10mL of pyridin...
Embodiment 3
[0112] Synthesis of Carborane-Perylene Diimide Derivatives (n=9 in this example)
[0113] Wherein the raw material selects m-iodoaniline, m-ethynyl aniline, and the alkyl ketone selects 12-tritricone;
[0114] (1) Synthesis of compound 1
[0115] Weigh 2.19g m-iodoaniline, 0.58g Pd(PPh 3 ) 4 , 0.095g CuI and 1.17g m-ethynylaniline were placed in a 100mL two-necked flask. Under nitrogen protection, 10 mL of triethylamine and 40 mL of tetrahydrofuran were sequentially added to the reaction system, heated to 60° C., stirred for 8 hours, cooled to room temperature, and spin-dried. A brown solid was obtained by column chromatography using dichloromethane:petroleum ether (1:1) as the eluent. The resulting solid was dried under vacuum at 40°C. Its reaction equation is as follows:
[0116]
[0117] (2) Synthesis of Compound 2
[0118] Weigh 3.39g of 12-docotriconone and 1.38g of hydroxylamine hydrochloride in a 100mL single-necked bottle, add 10mL of pyridine and 22mL of eth...
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