Soft matter, slow dynamics and art

2003 ◽  
Vol 2 (7) ◽  
pp. 427-429 ◽  
Author(s):  
Robert Steinberg
Keyword(s):  
2002 ◽  
Vol 123 ◽  
pp. 237-251 ◽  
Author(s):  
Luca Cipelletti ◽  
Laurence Ramos ◽  
S. Manley ◽  
E. Pitard ◽  
D. A. Weitz ◽  
...  
Keyword(s):  

Author(s):  
Tom McLeish

‘The science of softness’ provides a brief history and overview of soft matter science. The development of soft matter science was propelled by a combination of communication within the scientific community; intrinsic conceptual overlap and commonality; and visionary leadership from a small number of pioneering scientists. Chemistry proved as essential an ingredient to the new science of soft matter as ideas and techniques from physics. The characteristics of soft matter include motion; structure on intermediate length scales; slow dynamics; and universality. Microscopy is the most obvious and direct example of experimental tools applied across the gamut of soft materials.


2005 ◽  
Vol 17 (6) ◽  
pp. R253-R285 ◽  
Author(s):  
Luca Cipelletti ◽  
Laurence Ramos
Keyword(s):  

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Naoyuki Katayama ◽  
Keita Kojima ◽  
Tomoki Yamaguchi ◽  
Sosuke Hattori ◽  
Shinya Tamura ◽  
...  

AbstractElectronic instabilities in transition metal compounds often spontaneously form orbital molecules, which consist of orbital-coupled metal ions at low temperature. Recent local structural studies utilizing the pair distribution function revealed that preformed orbital molecules appear disordered even in the high-temperature paramagnetic phase. However, it is unclear whether preformed orbital molecules are dynamic or static. Here, we provide clear experimental evidence of the slow dynamics of disordered orbital molecules realized in the high-temperature paramagnetic phase of LiVS2, which exhibits vanadium trimerization upon cooling below 314 K. Unexpectedly, the preformed orbital molecules appear as a disordered zigzag chain that fluctuate in both time and space under electron irradiation. Our findings should advance studies on soft matter physics realized in an inorganic material due to disordered orbital molecules.


2020 ◽  
Author(s):  
Nipuna Weerasinghe ◽  
Steven Fried ◽  
Anna Eitel ◽  
Andrey Struts ◽  
Suchithranga Perera ◽  
...  

2020 ◽  
Author(s):  
Guanjun Deng ◽  
Xinghua Peng ◽  
Zhihong Sun ◽  
Wei Zheng ◽  
Jia Yu ◽  
...  

Nature has always inspired robotic designs and concepts. It is conceivable that biomimic nanorobots will soon play a prominent role in medicine. In this paper, we developed a natural killer cell-mimic AIE nanoterminator (NK@AIEdots) by coating natural kill cell membrane on the AIE-active polymeric endoskeleton, PBPTV, a highly bright NIR-II AIE-active conjugated polymer. Owning to the AIE and soft-matter characteristics of PBPTV, as-prepared nanoterminator maintained the superior NIR-II brightness (quantum yield ~8%) and good biocompatibility. Besides, they could serve as tight junctions (TJs) modulator to trigger an intracellular signaling cascade, causing TJs disruption and actin cytoskeleton reorganization to form intercellular “green channel” to help themselves crossing Blood-Brain Barriers (BBB) silently. Furthermore, they could initiatively accumulate to glioblastoma cells in the complex brain matrix for high-contrast and through-skull tumor imaging. The tumor growth was also greatly inhibited by these nanoterminator under the NIR light illumination. As far as we known, The QY of PBPTV is the highest among the existing NIR-II luminescent conjugated polymers. Besides, the NK-cell biomimetic nanorobots will open new avenue for BBB-crossing delivery.


2019 ◽  
Author(s):  
Ayumu Karimata ◽  
Pradnya Patil ◽  
Eugene Khaskin ◽  
Sébastien Lapointe ◽  
robert fayzullin ◽  
...  

Direct translation of mechanical force into changes in chemical behavior on a molecular level has important implication not only for the fundamental understanding of mechanochemical processes, but also for the development of new stimuli-responsive materials. In particular, detection of mechanical stress in polymers via non-destructive methods is important in order to prevent material failure and to study the mechanical properties of soft matter. Herein, we report that highly sensitive changes in photoluminescence intensity can be observed in response to the mechanical stretching of cross-linked polymer films when using stable, (pyridinophane)Cu-based dynamic mechanophores. Upon stretching, the luminescence intensity increases in a fast and reversible manner even at small strain (< 50%) and applied stress (< 0.1 MPa) values. Such sensitivity is unprecedented when compared to previously reported systems based on organic mechanophores. The system also allows for the detection of weak mechanical stress by spectroscopic measurements or by direct visual methods.<br>


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