scholarly journals Structure–activity relationship for the solid state emission of a new family of “push–pull” π-extended chromophores

2017 ◽  
Vol 196 ◽  
pp. 143-161 ◽  
Author(s):  
Andrea Nitti ◽  
Francesca Villafiorita-Monteleone ◽  
Aurora Pacini ◽  
Chiara Botta ◽  
Tersilla Virgili ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Optical Properties ◽  
Solid State ◽  
Substituted Benzenes ◽  
Design Synthesis ◽  
Structure Building ◽  
New Family ◽  
Structure Activity ◽  
Comprehensive Picture ◽  
Cyano Groups

We report the design, synthesis, molecular optical properties, and solid state emissive behaviour of a series of novel compounds, which, similar to the archetypal AIE luminogen tetraphenylethene, are formed of a central olefin stator and decorated with either three or four rotors. These rotors, being either electron-rich substituted benzenes, or electron-withdrawing functional groups (esters, ketones, cyano groups) confer a “push–pull” character to the overall molecular structure. Building on both new and already published contributions, a comprehensive picture of the properties and the potential of these compounds is provided.

Tuning the optical properties of N-aryl benzothiadiazole via Cu(ii)-catalyzed intramolecular C–H amination: the impact of the molecular structure on aggregation and solid state luminescence

2020 ◽  
Vol 7 (23) ◽  
pp. 3853-3861
Author(s):  
Yingnan Zhao ◽  
Jie Ding ◽  
Xiao Han ◽  
Ting Geng ◽  
Xiuwen Zhou ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Optical Properties ◽  
Solid State ◽  
Optical Performance ◽  
Subtle Change ◽  
The Impact ◽  
State Luminescence

The optical performance of 1–3 was influenced by the subtle change of the molecular structure as expected.

Development of Novel Glitazones as Antidiabetic Agents: Molecular Design, Synthesis, Evaluation of Glucose Uptake Activity and SAR Studies

2020 ◽  
Vol 17 (7) ◽  
pp. 840-849
Author(s):  
Mahendra Gowdru Srinivas ◽  
Prabitha Prabhakaran ◽  
Subhankar Probhat Mandal ◽  
Yuvaraj Sivamani ◽  
Pranesh Guddur ◽  
...  
Keyword(s):  
Glucose Uptake ◽  
Molecular Design ◽  
Docking Studies ◽  
Antidiabetic Activity ◽  
Design Synthesis ◽  
In Silico Docking ◽  
Ppar Γ ◽  
Sar Studies ◽  
Structure Activity ◽  
Uptake Activity

Background: Thiazolidinediones and its bioisostere, namely, rhodanines have become ubiquitous class of heterocyclic compounds in drug design and discovery. In the present study, as part of molecular design, a series of novel glitazones that are feasible to synthesize in our laboratory were subjected to docking studies against PPAR-γ receptor for their selection. Methods and Results: As part of the synthesis of selected twelve glitazones, the core moiety, pyridine incorporated rhodanine was synthesized via dithiocarbamate. Later, a series of glitazones were prepared via Knovenageal condensation. In silico docking studies were performed against PPARγ protein (2PRG). The titled compounds were investigated for their cytotoxic activity against 3T3-L1 cells to identify the cytotoxicity window of the glitazones. Further, within the cytotoxicity window, glitazones were screened for glucose uptake activity against L6 cells to assess their possible antidiabetic activity. Conclusion: Based on the glucose uptake results, structure activity relationships are drawn for the title compounds.

Quantum optics with nitrogen-vacancy centres in diamond

2017 ◽  
Author(s):  
Yiwen Chu ◽  
Mikhail D. Lukin
Keyword(s):  
Optical Properties ◽  
Quantum Information ◽  
Solid State ◽  
Quantum Optics ◽  
Quantum States ◽  
Nitrogen Vacancy ◽  
Common Theme ◽  
External Effects ◽  
Promising Candidate ◽  
Optical Photons

A common theme in the implementation of quantum technologies involves addressing the seemingly contradictory needs for controllability and isolation from external effects. Undesirable effects of the environment must be minimized, while at the same time techniques and tools must be developed that enable interaction with the system in a controllable and well-defined manner. This chapter addresses several aspects of this theme with regard to a particularly promising candidate for developing applications in both metrology and quantum information, namely the nitrogen-vacancy (NV) centre in diamond. The chapter describes how the quantum states of NV centres can be manipulated, probed, and efficiently coupled with optical photons. It also discusses ways of tackling the challenges of controlling the optical properties of these emitters inside a complex solid state environment.

scholarly journals Convenient Access to Functionalized Non-Symmetrical Atropisomeric 4,4′-Bipyridines

Compounds ◽  
2021 ◽  
Vol 1 (2) ◽  
pp. 58-74
Author(s):  
Emmanuel Aubert ◽  
Emmanuel Wenger ◽  
Paola Peluso ◽  
Victor Mamane
Keyword(s):  
Solid State ◽  
Intermolecular Interactions ◽  
Medicinal Chemistry ◽  
Crystal Packing ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Halogen Bonds ◽  
Cross Coupling Reactions ◽  
Cyano Groups ◽  
Post Functionalization

Non-symmetrical chiral 4,4′-bipyridines have recently found interest in organocatalysis and medicinal chemistry. In this regard, the development of efficient methods for their synthesis is highly desirable. Herein, a series of non-symmetrical atropisomeric polyhalogenated 4,4′-bipyridines were prepared and further functionalized by using cross-coupling reactions. The desymmetrization step is based on the N-oxidation of one of the two pyridine rings of the 4,4′-bipyridine skeleton. The main advantage of this methodology is the possible post-functionalization of the pyridine N-oxide, allowing selective introduction of chlorine, bromine or cyano groups in 2- and 2′-postions of the chiral atropisomeric 4,4′-bipyridines. The crystal packing in the solid state of some newly prepared derivatives was analyzed and revealed the importance of halogen bonds in intermolecular interactions.

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