Synthesis and Antimicrobial Assessment of Fe 3+ Inclusion Complex of p - tert -Butylcalix[4]arene Diamide Derivative
Present study deals with the synthesis of the p - tert -butylcalix[4]arene diamide derivative as ligand (L) and its Fe 3+ complex, followed by its characterization using TLC and FT-IR, while UV-Vis and Job’s plot study were performed for complex formation. Antimicrobial activity of the derivative (L...
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creator | Chandio, Anwar Ali Ali Memon, Ayaz Memon, Shahabuddin Memon, Fakhar N. Panhwar, Qadeer Khan Durmaz, Fatih Nizamani, Shafi Muhammad Brohi, Nazir Ahmed |
description | Present study deals with the synthesis of the
p
-
tert
-butylcalix[4]arene diamide derivative as ligand (L) and its Fe
3+
complex, followed by its characterization using TLC and FT-IR, while UV-Vis and Job’s plot study were performed for complex formation. Antimicrobial activity of the derivative (L) and its metal complex was carried out by the disc diffusion method against bacteria (
Escherichia coli
and
Staphylococcus albus
) and fungi (
R. stolonifer
). Different concentrations of the derivative (L) (6, 3, 1.5, 0.75, and 0.37
μ
g/mL) and its Fe
3+
complex were prepared, and Mueller–Hinton agar was used as the medium for the growth of microorganisms. Six successive dilutions of the derivative (L) and Fe
3+
complex were used against microorganisms. Two successive dilutions (6 and 3
μ
g/mL) of the derivative (L) showed antibacterial action against both Gram-positive and Gram-negative bacteria. In addition, three successive dilutions (6, 3, and 1.5
μ
g/mL) of the derivative (L) showed antifungal activity. However, all of six dilutions of the Fe
3+
complex showed antimicrobial activity. Derivative (L) showed 3 and 1.5
μ
g/mL minimum inhibitory concentrations (MIC) against bacteria and fungi, respectively. On the contrary, its Fe
3+
complex showed 0.37
μ
g/mL value of MIC against bacteria and fungi. Hence, Fe
3+
complex of the derivative (L) was found to be a more effective antimicrobial agent against selected bacteria and fungi than the diamide derivative (L). |
doi_str_mv | 10.1155/2019/2534072 |
format | Article |
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p
-
tert
-butylcalix[4]arene diamide derivative as ligand (L) and its Fe
3+
complex, followed by its characterization using TLC and FT-IR, while UV-Vis and Job’s plot study were performed for complex formation. Antimicrobial activity of the derivative (L) and its metal complex was carried out by the disc diffusion method against bacteria (
Escherichia coli
and
Staphylococcus albus
) and fungi (
R. stolonifer
). Different concentrations of the derivative (L) (6, 3, 1.5, 0.75, and 0.37
μ
g/mL) and its Fe
3+
complex were prepared, and Mueller–Hinton agar was used as the medium for the growth of microorganisms. Six successive dilutions of the derivative (L) and Fe
3+
complex were used against microorganisms. Two successive dilutions (6 and 3
μ
g/mL) of the derivative (L) showed antibacterial action against both Gram-positive and Gram-negative bacteria. In addition, three successive dilutions (6, 3, and 1.5
μ
g/mL) of the derivative (L) showed antifungal activity. However, all of six dilutions of the Fe
3+
complex showed antimicrobial activity. Derivative (L) showed 3 and 1.5
μ
g/mL minimum inhibitory concentrations (MIC) against bacteria and fungi, respectively. On the contrary, its Fe
3+
complex showed 0.37
μ
g/mL value of MIC against bacteria and fungi. Hence, Fe
3+
complex of the derivative (L) was found to be a more effective antimicrobial agent against selected bacteria and fungi than the diamide derivative (L).</description><identifier>ISSN: 2090-9063</identifier><identifier>EISSN: 2090-9071</identifier><identifier>DOI: 10.1155/2019/2534072</identifier><language>eng</language><ispartof>Journal of chemistry, 2019-03, Vol.2019, p.1-8</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c802-1604fab1ac9e241f8b837d416072c2864c711f9146324c252ca969ae000e9c403</citedby><cites>FETCH-LOGICAL-c802-1604fab1ac9e241f8b837d416072c2864c711f9146324c252ca969ae000e9c403</cites><orcidid>0000-0002-6088-8369</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Chandio, Anwar Ali</creatorcontrib><creatorcontrib>Ali Memon, Ayaz</creatorcontrib><creatorcontrib>Memon, Shahabuddin</creatorcontrib><creatorcontrib>Memon, Fakhar N.</creatorcontrib><creatorcontrib>Panhwar, Qadeer Khan</creatorcontrib><creatorcontrib>Durmaz, Fatih</creatorcontrib><creatorcontrib>Nizamani, Shafi Muhammad</creatorcontrib><creatorcontrib>Brohi, Nazir Ahmed</creatorcontrib><title>Synthesis and Antimicrobial Assessment of Fe 3+ Inclusion Complex of p - tert -Butylcalix[4]arene Diamide Derivative</title><title>Journal of chemistry</title><description>Present study deals with the synthesis of the
p
-
tert
-butylcalix[4]arene diamide derivative as ligand (L) and its Fe
3+
complex, followed by its characterization using TLC and FT-IR, while UV-Vis and Job’s plot study were performed for complex formation. Antimicrobial activity of the derivative (L) and its metal complex was carried out by the disc diffusion method against bacteria (
Escherichia coli
and
Staphylococcus albus
) and fungi (
R. stolonifer
). Different concentrations of the derivative (L) (6, 3, 1.5, 0.75, and 0.37
μ
g/mL) and its Fe
3+
complex were prepared, and Mueller–Hinton agar was used as the medium for the growth of microorganisms. Six successive dilutions of the derivative (L) and Fe
3+
complex were used against microorganisms. Two successive dilutions (6 and 3
μ
g/mL) of the derivative (L) showed antibacterial action against both Gram-positive and Gram-negative bacteria. In addition, three successive dilutions (6, 3, and 1.5
μ
g/mL) of the derivative (L) showed antifungal activity. However, all of six dilutions of the Fe
3+
complex showed antimicrobial activity. Derivative (L) showed 3 and 1.5
μ
g/mL minimum inhibitory concentrations (MIC) against bacteria and fungi, respectively. On the contrary, its Fe
3+
complex showed 0.37
μ
g/mL value of MIC against bacteria and fungi. Hence, Fe
3+
complex of the derivative (L) was found to be a more effective antimicrobial agent against selected bacteria and fungi than the diamide derivative (L).</description><issn>2090-9063</issn><issn>2090-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNo9kEtLw0AUhQdRsNTu_AGz19h55THLGK0WCi7sTiRMJjc4kkzCzLQ0_74JFs_mHM6FC-dD6J6SJ0rjeM0IlWsWc0FSdoUWjEgSSZLS6_-c8Fu08v6XTMoyHrN0gcLnaMMPeOOxsjXObTCd0a6vjGpx7j1434ENuG_wBjB_wFur24M3vcVF3w0tnObTgCMcwAUcPR_C2GrVmtOX-FYOLOAXozpTTw7OHFUwR7hDN41qPawuvkT7zeu-eI92H2_bIt9FOiMsogkRjaqo0hKYoE1WZTytxVSnTLMsETqltJFUJJwJzWKmlUykgmkdSC0IX6LHv7fTHu8dNOXgTKfcWFJSzszKmVl5YcbPCUBdTA</recordid><startdate>20190328</startdate><enddate>20190328</enddate><creator>Chandio, Anwar Ali</creator><creator>Ali Memon, Ayaz</creator><creator>Memon, Shahabuddin</creator><creator>Memon, Fakhar N.</creator><creator>Panhwar, Qadeer Khan</creator><creator>Durmaz, Fatih</creator><creator>Nizamani, Shafi Muhammad</creator><creator>Brohi, Nazir Ahmed</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-6088-8369</orcidid></search><sort><creationdate>20190328</creationdate><title>Synthesis and Antimicrobial Assessment of Fe 3+ Inclusion Complex of p - tert -Butylcalix[4]arene Diamide Derivative</title><author>Chandio, Anwar Ali ; Ali Memon, Ayaz ; Memon, Shahabuddin ; Memon, Fakhar N. ; Panhwar, Qadeer Khan ; Durmaz, Fatih ; Nizamani, Shafi Muhammad ; Brohi, Nazir Ahmed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c802-1604fab1ac9e241f8b837d416072c2864c711f9146324c252ca969ae000e9c403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chandio, Anwar Ali</creatorcontrib><creatorcontrib>Ali Memon, Ayaz</creatorcontrib><creatorcontrib>Memon, Shahabuddin</creatorcontrib><creatorcontrib>Memon, Fakhar N.</creatorcontrib><creatorcontrib>Panhwar, Qadeer Khan</creatorcontrib><creatorcontrib>Durmaz, Fatih</creatorcontrib><creatorcontrib>Nizamani, Shafi Muhammad</creatorcontrib><creatorcontrib>Brohi, Nazir Ahmed</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chandio, Anwar Ali</au><au>Ali Memon, Ayaz</au><au>Memon, Shahabuddin</au><au>Memon, Fakhar N.</au><au>Panhwar, Qadeer Khan</au><au>Durmaz, Fatih</au><au>Nizamani, Shafi Muhammad</au><au>Brohi, Nazir Ahmed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Antimicrobial Assessment of Fe 3+ Inclusion Complex of p - tert -Butylcalix[4]arene Diamide Derivative</atitle><jtitle>Journal of chemistry</jtitle><date>2019-03-28</date><risdate>2019</risdate><volume>2019</volume><spage>1</spage><epage>8</epage><pages>1-8</pages><issn>2090-9063</issn><eissn>2090-9071</eissn><abstract>Present study deals with the synthesis of the
p
-
tert
-butylcalix[4]arene diamide derivative as ligand (L) and its Fe
3+
complex, followed by its characterization using TLC and FT-IR, while UV-Vis and Job’s plot study were performed for complex formation. Antimicrobial activity of the derivative (L) and its metal complex was carried out by the disc diffusion method against bacteria (
Escherichia coli
and
Staphylococcus albus
) and fungi (
R. stolonifer
). Different concentrations of the derivative (L) (6, 3, 1.5, 0.75, and 0.37
μ
g/mL) and its Fe
3+
complex were prepared, and Mueller–Hinton agar was used as the medium for the growth of microorganisms. Six successive dilutions of the derivative (L) and Fe
3+
complex were used against microorganisms. Two successive dilutions (6 and 3
μ
g/mL) of the derivative (L) showed antibacterial action against both Gram-positive and Gram-negative bacteria. In addition, three successive dilutions (6, 3, and 1.5
μ
g/mL) of the derivative (L) showed antifungal activity. However, all of six dilutions of the Fe
3+
complex showed antimicrobial activity. Derivative (L) showed 3 and 1.5
μ
g/mL minimum inhibitory concentrations (MIC) against bacteria and fungi, respectively. On the contrary, its Fe
3+
complex showed 0.37
μ
g/mL value of MIC against bacteria and fungi. Hence, Fe
3+
complex of the derivative (L) was found to be a more effective antimicrobial agent against selected bacteria and fungi than the diamide derivative (L).</abstract><doi>10.1155/2019/2534072</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6088-8369</orcidid></addata></record> |
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title | Synthesis and Antimicrobial Assessment of Fe 3+ Inclusion Complex of p - tert -Butylcalix[4]arene Diamide Derivative |
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