17.6 Scheme for the click polymerization of diamines and bis(aroylace...Figure 17.7 Scheme for the click polymerization of diamines and bis(aroylace...Figure 17.8 Schematic illustration of spontaneous amino‐yne click reaction (...Figure 17.9 (a) Schematic procedures for the preparation of biomodification ...Figure 17.10 Schemes for the metal‐free polyhydrothiolation of dithiol and d...Figure 17.11 Schematics for catalyst‐free thiol‐yne click polymerization bet...Figure 17.12 Schematic illustration for metal‐free thiol‐yne reaction to mod...Figure 17.13 Syntheses of poly(vinylene ether ketone)s by organocatalytic ph...Figure 17.14 Schematic illustration for the strong organic base‐catalyzed po...Figure 17.15 Synthetic route employed for the modification of hydroxypropyl ...Figure 17.16 Rapid whole‐cell labeling and mapping of HeLa cells upon two mi...Figure 17.17 Specific labeling of Gram‐positive bacteria upon a two‐minute i...Figure 17.18 (a) Schematic illustration of the intracellular spontaneous ami...
18 Chapter 18Figure 18.1 Synthesis and photophysical property of BODIPY.Figure 18.2 Chemical structure, property of 1 and mechanism for TICT and AIE...Figure 18.3 Chemical structures of BODIPY derivatives 2–6 without othe...Figure 18.4 Chemical structures of TPE‐containing BODIPYs 7–10.Figure 18.5 Chemical structures of TPA‐containing BODIPYs 11–17.Figure 18.6 Chemical structures of benzodithiophene‐containing BODIPYs 18–23...Figure 18.7 Chemical structures of chiral BODIPYs 24–27.Figure 18.8 Chemical structures of metal‐containing BODIPYs 28–31.Figure 18.9 Chemical structures of BODIPY‐containing polymers 32–37.Figure 18.10 Chemical structures of other BODIPY derivatives 38–43.Figure 18.11 Chemical structures of other BODIPY analogues 44–49.Figure 18.12 Chemical structures of 50–52. Photoluminescence spectra o...Figure 18.13 Chemical structures of 53–57. Fluorescence photographs of...Figure 18.14 Chemical structures of 58, 59 and 60. (a) Absorption and (b) ph...Figure 18.15 Chemical structures of 61–63. (a) Absorption and (b) phot...Figure 18.16 Chemical structures of 64–65. Photoluminescence spectra o...Figure 18.17 Chemical structures of 66–69. Photoluminescence spectra of (a) Figure 18.18 Chemical structures of 70–73. (a) UV absorption spectrum ...Figure 18.19 Chemical structures of 7, 55, and 74. Photoluminescence spectra...Figure 18.20 Chemical structures of 7, 55, 75–78. Photoluminescence sp...Figure 18.21 Chemical structures of 79–85. Photoluminescence spectra i...Figure 18.22 Chemical structures of 86–92, Photoluminescence spectra i...Figure 18.23 Chemical structures of 93–96. Fluorescence spectra of (a)...Figure 18.24 Chemical structures of 97–101. Photoluminescence spectra ...Figure 18.25 (a) Photographic images of 44 in response to mechanical grindin...Figure 18.26 (a) Viscosity‐dependent fluorescence emission spectra of 21 in ...Figure 18.27 (a) The fluorescence emission property of 72 in thin film form ...Figure 18.28 (a) Color and (b) emission changes of 16 test strips before and...Figure 18.29 (a) Photograph of 40 powder under sunlight and UV light. (b) Th...Figure 18.30 Ultrafast and noninvasive long‐term bioimaging. (a) Long‐term c...Figure 18.31 Laser confocal fluorescence microscope photos of 15 coincubatio...Figure 18.32 Confocal images of HeLa cells after treatment with 38 and count...Figure 18.33 (a–d) Confocal fluorescence and bright‐field images of A549 cel...Figure 18.34 The mechanism for H2S‐mediated radiometric, NIR fluorescence li...Figure 18.35 (a) Absorption spectra recorded for 10 μM solutions of 2 upon a...
19 Chapter 19Figure 19.1 (a) Photoactivatable TPE‐C for photopatterning and anticounterfe...Figure 19.2 Photoactivable SCNPs by incorporation of silole molecules decora...Figure 19.3 (a) The photochromic mechanism of TPE‐chol and the bleaching pro...Figure 19.4 (a) The schematic illustration of photoactivatable mechanism bas...Figure 19.5 Photoactivable AIEgens based on (a) dihydro‐2‐azafluorenones and...Figure 19.6 (A) The chemical structure of photo‐switchable AIEgen of DSA‐2MC...Figure 19.7 The photo‐controlled photoacoustic and fluorescence transformati...Figure 19.8 (a) Optimized ground‐state geometries of o/c‐BTTE, o/c‐ABTE, o/c Figure 19.9 (A) The structure of P‐PHT and its emission behaviors in THF and...Figure 19.10 (a) Photochromic salicylaldehyde derivative TPENOEt between the...Figure 19.11 (a) Chemical structures of (Z)‐ and (E)‐TPE‐UPy with distinct a...Figure 19.12 (a) The chemical and single crystal structures of t‐FSBO, t‐2FS...Figure 19.13 (a) The AIEgen of Z‐MPPMNAN and its multiple photoreactions und...
20 Chapter 20Figure 20.1 Graphical representation of fluorescence property in naphthalimi...Figure 20.2 Representation of naphthalimide moiety demonstrating the most re...Figure 20.3 Examples of condensed‐state‐emitting naphthalimide derivatives w...Scheme 20.1 Common synthetic routes used in the generation of the AIE/AIEE‐a...Figure 20.4 Examples of condensed‐state‐emitting naphthalimide derivatives w...Figure 20.5 Examples of condensed‐state‐emitting naphthalimide derivatives w...Figure 20.6 Examples of condensed‐state‐emitting naphthalimide derivatives w...Figure 20.7 Examples of condensed‐state‐emitting naphthalimide derivatives w...Figure 20.8 Imaging by using the probe IV5. (a) Confocal fluorescence imagin...Figure 20.9 Examples of condensed‐state‐emitting naphthalimide derivatives w...Figure 20.10 Examples of condensed‐state‐emitting naphthalimide derivatives ...Figure 20.11 Thermocontrolled bilayer fluorescence pattern switching devices...
Guide
6 Preface to Handbook of Aggregation‐Induced Emission
7 Preface to Volume 2: Typical AIEgens Design
10 Index
11 WILEY END USER LICENSE AGREEMENT
Pages
1 iii
2 iv
3 xvii
4 xviii
5 xix
6 xx
7 xxi
8 xxiii
9 xxv