Synthesis OF Ligands O.F BIS-Oxadiazole Triazole Witb Open OR Close Sides and Their Complxes With (Ctlf, Pdll) -

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W.K. Me.hdi
F. H. Musa
H. A. Fadhel

Abstract

A  OUI,tiper  of LWW lig_;:tnds  .of  ppen sides. of Bis-'Oxad1azoJe· and·


Bis-triazole   derived from dichloroetbane  and  [Bis  0-ohloro   et!:ty)


= :=::                                                 =


ether)] (BCEE)' wersynthesi:zed. These inelude: 1, 4- bis[-3{thio- 2 -


 


. (Chloro·ethyl)l1 1;4 - oxadiazole ......$yl] butane (-L I);1  4 B'is {phenl-


3{thio - 2 ( 2 -chloroethoxy)- ethyl} 1 3A- oxadiazole-5yl)  butane (t2)'l His [4-_ph nyl -3{thio(chloro thy:l)}1; ,4 - ttiazoJ Syl]  methane (L1) Bis[ phehyl-3{, thi-0- 2( 2-chloroethoxy) ethyl}  1,,2:,4- triazole- 5yl]


: =


methane  (L:4)    1,. 2- bi[<.1- . pnenyl: -3 {tbio- 2 (cb.loroethy1}}  L,2,4-


 


triazo1e - 5yl]ethane;  :lll()T!O.di.mefuyl  sulphoxide  (Ls),  l,2- Bis  [4.­ pbenyl -3 {thio-  2( 2- chloroethoxy)  ethyl-} 1,2,4 - triazole - 5) ] ethane (L ) and 1,4 - Bis [4-phenyl """'"3    {thio-2 ..(chloroe-thyl)} 1,2,4-


triazole - SyL] butane; mono dimetby.ls Jiphoxide (L 7)   re pecti.vely.


Thi$ was  prepared £tom  the rea tiqn  of · one mple of  the fol'lowing


¢ompounds:  1, 4: - Hi\5 t2-thio- 1- 3.4 -oxadiazole  5yiJ ,butane (M.1), Bis- (4-phen:yl-3Ahio1-1 2.4 -friazole -S.ylmethane (M   2),   1, 2--  is (fhph·nyl-J- thiol-l ,t.4- triazci'le-5yl) ethane (fv[3) and  1 ,4His


[4-phenyl   -J.  - .t hio\  - 1.  2,  4  - tri l mle  - 5  ylJ butane . ( 4)


re-spectively \\lith two moleof qichl oethane and (BCEE)  and two


moles of s6dium  hydroxide. In. :adtt:ition   new c-lose  lig-ands of Bls­


o adiazofam;! B.is-triaz9-le derivati ves with !)ot;ne- of th. ir coro._pl es


bf coppei'· and palladium  were synthesLzed. The ligands.. were


 

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How to Cite
[1]
Me.hdi, W. et al. 2017. Synthesis OF Ligands O.F BIS-Oxadiazole Triazole Witb Open OR Close Sides and Their Complxes With (Ctlf, Pdll) -. Ibn AL-Haitham Journal For Pure and Applied Sciences. 21, 3 (Sep. 2017), 93–116.
Section
Chemistry

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