merocyanine dyes
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2021 ◽  
Vol 18 (8) ◽  
pp. 085001
Author(s):  
Niyazbek Ibrayev ◽  
Dmitriy Afanasyev ◽  
Alexander Ishchenko ◽  
Assel Kanapina

2021 ◽  
pp. 2100213
Author(s):  
Tim Schembri ◽  
Jin Hong Kim ◽  
Andreas Liess ◽  
Vladimir Stepanenko ◽  
Matthias Stolte ◽  
...  
Keyword(s):  

Author(s):  
Bernardino Tirri ◽  
Gloria Mazzone ◽  
Alistar Ottochian ◽  
Jerôme Gomar ◽  
Umberto Raucci ◽  
...  
Keyword(s):  

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Heinz Mustroph

Abstract Merocyanine dyes belong to the class of neutral polymethine dyes, where one terminal component is typically found in cyanine dyes and the second obtained from an active methylene compound. The different electron acceptor/donator abilities of the two terminal components have a marked impact on the electronic structure of a merocyanine dye and its equilibrium structure and electronic spectra. Their first technical application was spectral sensitization in silver halide photography. Today they have numerous of applications in textile dyeing and as membrane potential sensitive fluorescent dyes.


2021 ◽  
Author(s):  
Yulong Bai ◽  
Yanan Huang ◽  
Wang Wan ◽  
Wenhan Jin ◽  
Di Shen ◽  
...  

Protein misfolding and aggregation process involves local polarity and viscosity fluctuation. Herein we modulated the polarity and viscosity sensitivities of merocyanine dyes to detect protein aggregation. We demonstrated how structural...


Author(s):  
Abigail J. Van Riesen ◽  
Ryan E. Johnson ◽  
M. Sameer Al-Abdul-Wahid ◽  
Cristina Liota ◽  
Anjelyn Christyanton ◽  
...  

Synthesis ◽  
2020 ◽  
Vol 53 (02) ◽  
pp. 318-325
Author(s):  
Frank Würthner ◽  
Alhama Arjona-Esteban ◽  
Anja Rausch ◽  
Myroslav O. Vysotsky

We describe a synthetic method for the synthesis of merocyanine dyes containing a bridge with three conjugated double bonds. This method consists of two successive condensation reactions. The first one is made between CH-acidic indane-1,3-dione acceptor units and an appropriate ketone (here acetone or hexan-2-one). The extended acceptor thus obtained is condensed with an aldehyde in the next step. The dyes show high tinctorial strength due to intense absorption bands at wavelengths between 500 and 750 nm.


2020 ◽  
Vol 176 ◽  
pp. 108193
Author(s):  
Felipe Lange Coelho ◽  
Rodrigo da Costa Duarte ◽  
Cláudia de Ávila Braga ◽  
Josene Maria Toldo ◽  
Paulo Fernando Bruno Gonçalves ◽  
...  

2019 ◽  
Author(s):  
Chem Int

In this paper, synthesis of different classes of five/six membered heterocyclic cyanine dyes has been reviewed. In this paper review detailed synthesis steps were represented via equations. The synthesis covers, monomethine cyanine dyes (simple cyanine dyes), dimethine cyanine dyes, trimethine cyanine dyes (carbocyanine dyes), styryl cyanine dyes (hemicyanine dyes), aza-styryl cyanine dyes (aza-hemicyanine dyes and/or aza-cyanine dyes), merocyanine dyes (acyclic merocyanine dyes and cyclic merocyanine dyes) and apocyanine dyes. Besides, in the introduction section of this review paper some light is focused on the uses, applications and properties of cyanine dyes. This review paper is informative, useful and very readable for synthetic dye chemists, researchers and students who look for the different methods in the synthesis and preparation of various classes of five/six membered heterocyclic cyanine dyes with special emphasize in the field of heterocyclic and/or cyanine dyes chemistry. This specific type of collective review in the synthesis of different classes of only five/six membered heterocyclic cyanine dyes has been paid little attention and has great importance in the chemistry literature.


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