Synthesis of Naphthocyclobutenes from α-Naphthyl Acrylates by Visible-Light Energy-Transfer Catalysis

2019 ◽  
Vol 21 (11) ◽  
pp. 4365-4369 ◽  
Author(s):  
Theodor Peez ◽  
Veronika Schmalz ◽  
Klaus Harms ◽  
Ulrich Koert
2019 ◽  
Vol 7 (7) ◽  
pp. 1801229 ◽  
Author(s):  
Gwang‐Hun Jung ◽  
SeokJae Yoo ◽  
Jin‐Soo Kim ◽  
Q‐Han Park

2019 ◽  
Author(s):  
Tuhin Patra ◽  
Satobhisha Mukherjee ◽  
Jiajia Ma ◽  
Felix Strieth-Kalthoff ◽  
Frank Glorius

<sub>A general strategy to access both aryl and alkyl radicals by photosensitized decarboxylation of the corresponding carboxylic acids esters has been developed. An energy transfer mediated homolysis of unsymmetrical sigma-bonds for a concerted fragmentation/decarboxylation process is involved. As a result, an independent aryl/alkyl radical generation step enables a series of key C-X and C-C bond forming reactions by simply changing the radical trapping agent.</sub>


2021 ◽  
Vol 118 (42) ◽  
pp. e2104481118
Author(s):  
Jintao Tong ◽  
Dalei Wang ◽  
Ye Liu ◽  
Xin Lou ◽  
Jiwei Jiang ◽  
...  

In nature, microorganisms could sense the intensity of the incident visible light and exhibit bidirectional (positive or negative) phototaxis. However, it is still challenging to achieve the similar biomimetic phototaxis for the artificial micro/nanomotor (MNM) counterparts with the size from a few nanometers to a few micrometers. In this work, we report a fuel-free carbon nitride (C3N4)/polypyrrole nanoparticle (PPyNP)-based smart MNM operating in water, whose behavior resembles that of the phototactic microorganism. The MNM moves toward the visible light source under low illumination and away from it under high irradiation, which relies on the competitive interplay between the light-induced self-diffusiophoresis and self-thermophoresis mechanisms concurrently integrated into the MNM. Interestingly, the competition between these two mechanisms leads to a collective bidirectional phototaxis of an ensemble of MNMs under uniform illuminations and a spinning schooling behavior under a nonuniform light, both of which can be finely controllable by visible light energy. Our results provide important insights into the design of the artificial counterpart of the phototactic microorganism with sophisticated motion behaviors for diverse applications.


2014 ◽  
Vol 115 (22) ◽  
pp. 224308 ◽  
Author(s):  
Lei Yang ◽  
Jiazhang Dong ◽  
Zhongcheng Jiang ◽  
Anlian Pan ◽  
Xiujuan Zhuang

2020 ◽  
Author(s):  
Katie Rykaczewski ◽  
Corinna Schindler

<div> <p>One of the most efficient ways to synthesize oxetanes is the light-enabled [2+2] cycloaddition reaction of carbonyls and alkenes, referred to as the Paternò-Büchi reaction. The reaction conditions for this transformation typically require the use of high energy UV light to excite the carbonyl, limiting the applications, safety, and scalability. We herein report the development of a visible light-mediated Paternò-Büchi reaction protocol that relies on triplet energy transfer from an iridium-based photocatalyst to the carbonyl substrates. This mode of activation is demonstrated for a variety of aryl glyoxylates and negates the need for both, visible light-absorbing carbonyl starting materials or UV light to enable access to a variety of functionalized oxetanes in up to 99% yield.</p> </div> <br>


LASER THERAPY ◽  
1995 ◽  
Vol 7 (3) ◽  
pp. 101-105 ◽  
Author(s):  
R. Lubart ◽  
H. Friedmann ◽  
M. Sinykov ◽  
N. Grossman
Keyword(s):  

2019 ◽  
Vol 2020 (10) ◽  
pp. 1478-1481 ◽  
Author(s):  
Sapna Ahuja ◽  
Steffen Jockusch ◽  
Angel Ugrinov ◽  
Jayaraman Sivaguru

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