Handbook of Aggregation-Induced Emission, Volume 2. Группа авторов

Handbook of Aggregation-Induced Emission, Volume 2 - Группа авторов


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Liang C, Jiang S. Fluorescence light‐up detection of cyanide in water based on cyclization reaction followed by ESIPT and AIEE. Analyst (Cambridge, UK) 2017; 142(24):4825–33.

      35 35 Pham X‐Q, Kumar N, Ha‐Thi M‐H, Leray I. Sensitive and selective detection of uranyl ions based on aggregate‐breaking mechanism. J. Photochem. Photobiol. A. 2019; 373:139–45.

      36 36 Wang Z, Zhou F, Wang J, Zhao Z, Qin A, Yu Z, et al. Electronic effect on the optical properties and sensing ability of AIEgens with ESIPT process based on salicylaldehyde azine. Sci. China: Chem. 2018; 61(1):76–87.

      37 37 Xie Y, Yan L, Tang Y, Tang M, Wang S, Bi L, et al. A smart fluorescent probe based on salicylaldehyde Schiff's base with AIE and ESIPT characteristics for the detections of N2H4 and ClO. J. Fluoresc. 2019; 29(2):399–406.

      38 38 Liu L, Wu B, Yu P, Zhuo R‐X, Huang S‐W. Sub‐20 nm nontoxic aggregation‐induced emission micellar fluorescent light‐up probe for highly specific and sensitive mitochondrial imaging of hydrogen sulfide. Polym. Chem. 2015; 6(29):5185–9.

      39 39 Liu H, Wei R, Xiang Y, Tong A. Fluorescence turn‐on detection of pyrophosphate based on aggregation‐induced emission property of 5‐chlorosalicylaldehyde azine. Anal. Meth. 2015; 7(2):753–8.

      40 40 Liu H, Wang X, Xiang Y, Tong A. Fluorescence turn‐on detection of cysteine over homocysteine and glutathione based on “ESIPT” and “AIE”. Anal. Meth. 2015; 7(12):5028–33.

      41 41 Song H, Zhou Y, Qu H, Xu C, Wang X, Liu X, et al. A novel AIE plus ESIPT fluorescent probe with a large Stokes shift for cysteine and homocysteine: application in cell imaging and portable kit. Ind. Eng. Chem. Res. 2018; 57(44):15216–23.

      42 42 Chen X, Xiang Y, Li N, Song P, Tong A. Fluorescence turn‐on detection of protamine based on aggregation‐induced emission enhancement characteristics of 4‐(6'‐carboxyl)hexyloxysalicylaldehyde azine. Analyst 2010; 135(5):1098–105.

      43 43 Chen X, Xiang Y, Tong A. Facile, sensitive and selective fluorescence turn‐on detection of HSA/BSA in aqueous solution utilizing 2,4‐dihydroxyl‐3‐iodo salicylaldehyde azine. Talanta 2010; 80(5):1952–8.

      44 44 Peng L, Wei R, Li K, Zhou Z, Song P, Tong A. A ratiometric fluorescent probe for hydrophobic proteins in aqueous solution based on aggregation‐induced emission. Analyst (Cambridge, UK) 2013; 138(7):2068–72.

      45 45 Peng L, Gao M, Cai X, Zhang R, Li K, Feng G, et al. A fluorescent light‐up probe based on AIE and ESIPT processes for β‐galactosidase activity detection and visualization in living cells. J. Mater. Chem. B. 2015; 3(47):9168–72.

      46 46 Peng L, Xiao L, Ding Y, Xiang Y, Tong A. A simple design of fluorescent probes for indirect detection of β‐lactamase based on AIE and ESIPT processes. J. Mater. Chem. B. 2018; 6(23):3922–6.

      47 47 Peng L, Xu S, Zheng X, Cheng X, Zhang R, Liu J, et al. Rational design of a red‐emissive fluorophore with AIE and ESIPT characteristics and its application in light‐up sensing of esterase. Anal. Chem. 2017; 89(5):3162–8.

      48 48 Liu H, Song P, Wei R, Li K, Tong A. A facile, sensitive and selective fluorescent probe for heparin based on aggregation‐induced emission. Talanta 2014; 118:348–52.

      49 49 Song P, Chen X, Xiang Y, Huang L, Zhou Z, Wei R, et al. A ratiometric fluorescent pH probe based on aggregation‐induced emission enhancement and its application in live‐cell imaging. J. Mater. Chem. 2011; 21(35):13470–5.

      50 50 Ma X, Cheng J, Liu J, Zhou X, Xiang H. Ratiometric fluorescent pH probes based on aggregation‐induced emission‐active salicylaldehyde azines. N. J. Chem. 2015; 39(1):492–500.

      51 51 Kachwal V, Vamsi Krishna IS, Fageria L, Chaudhary J, Kinkar Roy R, Chowdhury R, et al. Exploring the hidden potential of a benzothiazole‐based Schiff‐base exhibiting AIE and ESIPT and its activity in pH sensing, intracellular imaging and ultrasensitive & selective detection of aluminium (Al3+). Analyst 2018; 143(15):3741–8.

      52 52 Li K, Feng Q, Niu G, Zhang W, Li Y, Kang M, et al. Benzothiazole‐based AIEgen with tunable excited‐state intramolecular proton transfer and restricted intramolecular rotation processes for highly sensitive physiological pH sensing. ACS Sens. 2018; 3(5):920–8.

      53 53 Li K, Wang J, Li Y, Si Y, He J, Meng X, et al. Combining two different strategies to overcome the aggregation caused quenching effect in the design of ratiometric fluorescence chemodosimeters for pH sensing. Sens. Actuat. B. 2018; 274:654–61.

      54 54 Shuai Z, Peng Q. Organic light‐emitting diodes: theoretical understanding of highly efficient materials and development of computational methodology. Natl. Sci. Rev. 2016; 4(2):224–39.

      55 55 Liang J, Tang BZ, Liu B. Specific light‐up bioprobes based on AIEgen conjugates. Chem. Soc. Rev. 2015; 44(10):2798–11.

      56 56 Hu Q, Gao M, Feng G, Liu B. Mitochondria‐targeted cancer therapy using a light‐up probe with aggregation‐induced‐emission characteristics. Ang. Chem. Int. Ed. 2014; 53(51):14225–9.

      57 57 Chen X, Li Y, Li S, Gao M, Ren L, Tang BZ. Mitochondria‐ and lysosomes‐targeted synergistic chemo‐photodynamic therapy associated with self‐monitoring by dual light‐up fluorescence. Adv. Funct. Mater. 2018; 28(44):1804362.

      58 58 Green DR, Reed JC. Mitochondria and apoptosis. Science. 1998; 281(5381):1309–12.

      59 59 Gao M, Sim CK, Leung CWT, Hu Q, Feng G, Xu F, et al. A fluorescent light‐up probe with AIE characteristics for specific mitochondrial imaging to identify differentiating brown adipose cells. Chem. Commun. 2014; 50(61):8312–5.

      60 60 Xu J‐L, Quan Y, Li Q‐Y, Lu H, Wu H, Yin J, et al. Significant emission enhancement of a bola‐amphiphile with salicylaldehyde azine moiety induced by the formation of [2]pseudorotaxane with γ‐cyclodextrin. RSC Adv. 2015; 5(107):88176–80.

      61 61 Nunes da Silva R, Costa CC, Santos MJG, Alves MQ, Braga SS, Vieira SI, et al. Fluorescent light‐up probe for the detection of protein aggregates. Chem. Asian J. 2019; 14(6):859–63.

      62 62 Gao M, Hu Q, Feng G, Tang BZ, Liu B. A fluorescent light‐up probe with “AIE + ESIPT” characteristics for specific detection of lysosomal esterase. J. Mater. Chem. B. 2014; 2(22):3438–42.

      63 63 Hu Q, Gao M, Feng G, Chen X, Liu B. A cell apoptosis probe based on fluorogen with aggregation induced emission characteristics. ACS Appl. Mater. Interf. 2015; 7(8):4875–82.

      64 64 Gao M, Hu Q, Feng G, Tomczak N, Liu R, Xing B, et al. A multifunctional probe with aggregation‐induced emission characteristics for selective fluorescence imaging and photodynamic killing of bacteria over mammalian cells. Adv. Health. Mat. 2015; 4(5):659–63.

      65 65 Gao M, Wang L, Chen J, Li S, Lu G, Wang L, et al. Aggregation‐induced emission active probe for light‐up detection of anionic surfactants and wash‐free bacterial imaging. Chem. Eur. J. 2016; 22(15):5107–12.

      66 66 Leung CWT, Wang Z, Zhao E, Hong Y, Chen S, Kwok RTK, et al. A lysosome‐targeting AIEgen for autophagy visualization. Adv. Health. Mater. 2016; 5(4):427–31.

      67 67 Wang Z, Gui C, Zhao E, Wang J, Li X, Qin A, et al. Specific fluorescence probes for lipid droplets based on simple AIEgens. ACS Appl. Mater. Interf. 2016; 8(16):10193–200.

      68 68 Kwon JE, Park SY. Advanced organic optoelectronic materials: harnessing excited‐state intramolecular proton transfer (ESIPT) process. Adv. Mater. 2011; 23(32):3615–42.

      69 69 Dick B, Ernsting NP. Excited‐state intramolecular proton transfer in 3‐hydroxylflavone isolated in solid argon: fluoroescence and fluorescence‐excitation spectra and tautomer fluorescence rise time. J. Phys. Chem. 1987; 91(16):4261–5.

      70 70 Chen X‐T, Xiang Y, Song P‐S, Wei R‐R, Zhou Z‐J, Li K, et al. p‐Carboxyl‐N‐salicylideneanilines: simple but efficient chromophores for one‐dimensional microrods with aggregation‐induced emission enhancement (AIEE) characteristics. J. Lumin. 2011; 131(7):1453–9.

      71 71 Cai M, Gao Z, Zhou X, Wang X, Chen S, Zhao Y, et al. A small change in molecular structure, a big difference in the


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