Conjugated rod–coil block copolymers: Synthesis, morphology, photophysical properties, and stimuli-responsive applications

2011 ◽  
Vol 36 (5) ◽  
pp. 603-637 ◽  
Author(s):  
Cheng-Liang Liu ◽  
Chia-Hung Lin ◽  
Chi-Ching Kuo ◽  
Sung-Tso Lin ◽  
Wen-Chang Chen
2018 ◽  
Author(s):  
Mustapha Abdu-Aguye ◽  
Nutifafa Doumon ◽  
Ivan Terzic ◽  
Vincent Voet ◽  
Katya Loos ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-24 ◽  
Author(s):  
Carmen Cretu ◽  
Loredana Maiuolo ◽  
Domenico Lombardo ◽  
Elisabeta I. Szerb ◽  
Pietro Calandra

The involvement of metal ions within the self-assembly spontaneously occurring in surfactant-based systems gives additional and interesting features. The electronic states of the metal, together with the bonds that can be established with the organic amphiphilic counterpart, are the factors triggering new photophysical properties. Moreover, the availability of stimuli-responsive supramolecular amphiphile assemblies, able to disassemble in a back-process, provides reversible switching particularly useful in novel approaches and applications giving rise to truly smart materials. In particular, small amphiphiles with an inner distribution, within their molecular architecture, of various polar and apolar functional groups, can give a wide variety of interactions and therefore enriched self-assemblies. If it is joined with the opportune presence and localization of noble metals, whose chemical and photophysical properties are undiscussed, then very interesting materials can be obtained. In this minireview, the basic concepts on self-assembly of small amphiphilic molecules with noble metals are shown with particular reference to the photophysical properties aiming at furnishing to the reader a panoramic view of these exciting problematics. In this respect, the following will be shown: (i) the principles of self-assembly of amphiphiles that involve noble metals, (ii) examples of amphiphiles and amphiphile-noble metal systems as representatives of systems with enhanced photophysical properties, and (iii) final comments and perspectives with some examples of modern applications.


2021 ◽  
Vol 9 (1) ◽  
pp. 38-50
Author(s):  
Hien Phan ◽  
Vincenzo Taresco ◽  
Jacques Penelle ◽  
Benoit Couturaud

Stimuli-responsive amphiphilic block copolymers obtained by PISA have emerged as promising nanocarriers for enhancing site-specific and on-demand drug release in response to a range of stimuli such as pH, redox agents, light or temperature.


2012 ◽  
Vol 24 (41) ◽  
pp. 5559-5563 ◽  
Author(s):  
Christoph Tonhauser ◽  
Ali A. Golriz ◽  
Christian Moers ◽  
Rebecca Klein ◽  
Hans-Jürgen Butt ◽  
...  

2020 ◽  
Vol 56 (55) ◽  
pp. 7633-7636 ◽  
Author(s):  
Laxmi Raman Adil ◽  
Parameswar Krishnan Iyer

A simple design strategy to convert ACQ materials into bright AIE luminogens is demonstrated. Unique differences in photophysical properties were observed among them which gave rise to stimuli responsive behaviour and sensor for chemical warfare agents.


2019 ◽  
Vol 77 (11) ◽  
pp. 5783-5810 ◽  
Author(s):  
Mehul Khimani ◽  
Hiren Patel ◽  
Vijay Patel ◽  
Paresh Parekh ◽  
Rohit L. Vekariya

Synlett ◽  
2020 ◽  
Vol 31 (17) ◽  
pp. 1663-1680 ◽  
Author(s):  
Tatsuya Nabeshima ◽  
Yusuke Chiba ◽  
Takashi Nakamura ◽  
Ryota Matsuoka

The dipyrrin–metal complexes and especially the boron complex 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) have recently attracted considerable attention because of their interesting properties and possible applications. We have developed two unique and useful ways to extend versatility and usefulness of the dipyrrin complexes. The first one is the linear and macrocyclic oligomerization of the BODIPY units. These arrangements of the B–F moieties of the oligomerized BODIPY units provide sophisticated functions, such as unique recognition ability toward cationic guest, associated with changes in the photophysical properties by utilizing unprecedented interactions between the B–F and a cationic species. The second one is introduction of additional ligating moieties into the dipyrrin skeleton. The multidentate N2Ox dipyrrin ligands thus obtained form a variety of complexes with 13 and 14 group elements, which are difficult to synthesize using the original N2 dipyrrin derivatives. Interestingly, these unique complexes exhibit novel structures, properties, and functions such as guest recognition, stimuli-responsive structural conversion, switching of the optical properties, excellent stability of the neutral radicals, etc. We believe that these multifunctional dipyrrin complexes will advance the basic chemistry of the dipyrrin complexes and develop their applications in the materials and medicinal chemistry fields.1 Introduction2 Linear Oligomers of Boron–Dipyrrin Complexes3 Cyclic Oligomers of Boron–Dipyrrin Complexes4 A Cyclic Oligomer of Zinc–Dipyrrin Complexes5 Group 13 Element Complexes of N2Ox Dipyrrins6 Chiral N2 and N2Ox Dipyrrin Complexes7 Group 14 Element Complexes of N2O2 Dipyrrins8 Other N2O2 Dipyrrin Complexes with Unique Properties and Functions9 Conclusion


2019 ◽  
Vol 10 (41) ◽  
pp. 5602-5616 ◽  
Author(s):  
Felix Wendler ◽  
Jessica C. Tom ◽  
Felix H. Schacher

Photoacids experience a strong increase in acidity when absorbing light and, hence, can be considered as molecular switches. The incorporation into amphiphilic block copolymers leads to novel stimuli-responsive materials with great potential.


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