Turn-on fluorescent sensor for the detection of cyanide based on a novel dicyanovinyl phenylacetylene

2017 ◽  
Vol 41 (10) ◽  
pp. 4058-4064 ◽  
Author(s):  
Eknarin Thanayupong ◽  
Khomson Suttisintong ◽  
Mongkol Sukwattanasinitt ◽  
Nakorn Niamnont

A novel phenylacetylene derivative (3) was successfully synthesized via Sonogashira coupling and a Knoevenagel reaction for cyanide ion detection.

2017 ◽  
Vol 27 (6) ◽  
pp. 2201-2212 ◽  
Author(s):  
Weerachai Nasomphan ◽  
Pramuan Tangboriboonrat ◽  
Srung Smanmoo

2021 ◽  
Author(s):  
Yasuhiro Morikawa ◽  
Miku Hirabara ◽  
Keiji Nishiwaki ◽  
Shigeo Suzuki ◽  
Isao Nakanishi

A new fluorescent sensor combining phenothiazine and indolium, which reacts specifically with the cyanide ion with a large Stokes shift and a good fluorescence quantum yield, was prepared. When CN-.


2021 ◽  
Author(s):  
Sudha Lakshminarayanan ◽  
Kumaresan.M Murugesan ◽  
Vanthana Jeyasingh ◽  
Narayanan Selvapalam ◽  
Geetha Dass

Abstract We have prepared and reporting a new cyanide colorimetric and turn-on fluorescent chemo sensor L. Naked-eye colorimetric studies shows the prepared receptor is selectively sensing cyanide ion in acetonitrile medium. The sensor L shows very weak fluorescence in acetonitrile medium. The emission intensity of L gets reduced (quenching of fluorescence) upon addition of one equivalent of cyanide. Meanwhile further gradual addition of more than one equivalents of cyanide onto 1:1 cyanide complex of L shows remarkable fluorescence enhancement. The weakly emissive receptor L show drastic enhancement in fluorescence intensity upon addition of excessive cyanide ion which is mainly attributed due to the restriction of intramolecular rotation of 1:1 L•CN- complex and intermolecular aggregation of host: guest complex. This enhanced fluorescence emission is attributed due to the aggregation induced enhanced emission (AIEE) is subsequently supported with UV-Vis, emission and 1H-NMR spectroscopic studies. The preferential binding of cyanide by electron deficient receptor L through hydrogen bonding and anion···π interaction over benzene analogue of L is also analyzed with help of MEP surface analyses. To the best of our knowledge, this is the first example for selective colorimetric and turn- on cyanide sensor through AIEE mechanism. This type of fluorine rich organic material having such an aggregation enhanced emission properties in response to cyanide addition will be useful to construct the new type of material for various sensory applications.


RSC Advances ◽  
2021 ◽  
Vol 11 (32) ◽  
pp. 19747-19754
Author(s):  
Pengfei Wang ◽  
Fanda Meng ◽  
Hao Su ◽  
Lijie Liu ◽  
Maroof Ahmad Khan ◽  
...  

In this work, a highly selective water-soluble “turn-on” fluorescent sensor for gallium ion recognition was reported.


Author(s):  
Mahesh Gosi ◽  
Nagaraju Marepu ◽  
Yeturu Sunandamma

ACS Sensors ◽  
2021 ◽  
Author(s):  
Pawan Thapa ◽  
Nicholas K. Byrnes ◽  
Alena A. Denisenko ◽  
James X. Mao ◽  
Austin D. McDonald ◽  
...  

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