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Volume 7

Biosensors Journal

ISSN: 2090-4967

Electrochemistry 2018

June 11-12, 2018

June 11-12, 2018 | Rome, Italy

4

th

International Conference on

Electrochemistry

Electrochemical thiocyanation of aromatic and alkene derivatives

James Y. Becker, Avishai Levy

and

Anna Gitkis

Ben-Gurion University of the Negev, Israel

T

he anodic thiocyanation of aromatic compounds [1, 2] showed both regio- and isomer- selectivity. For example, the para-

thiocyanate isomer was formed exclusively:

SCN- - e → SCN.

2SCN. → (SCN)2

The one-pot anodic thiocyanation and isothiocyanation of alkenes in both acidic two-phase (water-dichloromethane) and

homogeneous one-phase (water-acetonitrile) media will be described too [3, 4]. A selected example of type of products

obtained is illustrated in the scheme below:

becker@bgu.ac.il

Biosens J 2018, Volume 7

DOI: 10.4172/2090-4967-C1-003

OCH

3

OCH

3

SCN

(SCN)

2

+ polymer (SCN)

n

Anode

Me

Me

Me

Me

C C

N

CS

S

CN

Me

Me

Me

Me

C C

S

CN

S

CN

Me

Me

Me

Me

Me

CH

2

OH

Me

Me

C C

OH

S

CN

Me

Me

Me

Me

(1)

(Major)

(2)

(5)

(3)

C C

H

S

CN

Me

Me

Me

Me

(4)

(

trace)

C anode/[SCN]

-

DCM-H

2

O

0.5NH

2

SO

4