Preparation and crystallographic studies of a new mercuric salicylaldimine complex for fabrication of microscaled and nanoscaled mercuric sulfide as antimicrobial agents against human pathogenic yeasts and filamentous fungi. (16th December 2020)
- Record Type:
- Journal Article
- Title:
- Preparation and crystallographic studies of a new mercuric salicylaldimine complex for fabrication of microscaled and nanoscaled mercuric sulfide as antimicrobial agents against human pathogenic yeasts and filamentous fungi. (16th December 2020)
- Main Title:
- Preparation and crystallographic studies of a new mercuric salicylaldimine complex for fabrication of microscaled and nanoscaled mercuric sulfide as antimicrobial agents against human pathogenic yeasts and filamentous fungi
- Authors:
- Ibrahim, Ahmed B.M.
Mahmoud, Ghada Abd‐Elmonsef
Meurer, Florian
Bodensteiner, Michael - Abstract:
- Abstract : The new mercuric complex [Hg(HL)2 Cl2 ] incorporating salicylaldimine ligand (HL = 2‐((pyridin‐3‐ylimino)methyl)phenol) was fabricated where the ligand molecules behaved in a monodentate manner via their pyridine nitrogen atoms. In addition to elemental characterization, X‐ray crystallographic studies of the complex revealed its packing in a monoclinic crystal system (space group: I 2/ a, a = 13.4276(2) Å, b = 6.20950(10) Å, c = 27.7530 (4) Å, α = γ = 90°, and β = 98.1610(10)°). Hydrothermal treatment of [Hg(HL)2 Cl2 ] with thioacetamide afforded HgS microparticles (HgS μPs; Brunauer–Emmett–Teller [BET] surface area = 6.205 m 2 /g, diameter = 196.53–259.13 nm, and average size = 213.27 nm), whereas these microparticles were transformed to nanoscaled HgS particles (HgS NPs; BET surface area = 14.380 m 2 /g, diameter = 58.87–90.56 nm, and average size = 72.78 nm) by the action of ultrasonication. The as‐prepared HgS, HgS NPs in particular, afforded remarkable microbicidal activity against eight strains of filamentous and unicellular human pathogenic fungi and yeasts in comparison with cycloheximide. Remarkably, Aspergillus terreus grew up to 34.7 ± 1.88 mm in the absence of any fungicide, but HgS μPs, HgS NPs, and cycloheximide limited the fungal growth to 26 ± 0.94, 12.33 ± 1.6, and 28.3 ± 1.7 mm after incubation for 6 days. Besides, inhibition of Rhodotorula glutinis was of 7.6 ± 0.01 × 10 7 CFU/ml in control sample, but experiments included HgS μPs, HgS NPs, andAbstract : The new mercuric complex [Hg(HL)2 Cl2 ] incorporating salicylaldimine ligand (HL = 2‐((pyridin‐3‐ylimino)methyl)phenol) was fabricated where the ligand molecules behaved in a monodentate manner via their pyridine nitrogen atoms. In addition to elemental characterization, X‐ray crystallographic studies of the complex revealed its packing in a monoclinic crystal system (space group: I 2/ a, a = 13.4276(2) Å, b = 6.20950(10) Å, c = 27.7530 (4) Å, α = γ = 90°, and β = 98.1610(10)°). Hydrothermal treatment of [Hg(HL)2 Cl2 ] with thioacetamide afforded HgS microparticles (HgS μPs; Brunauer–Emmett–Teller [BET] surface area = 6.205 m 2 /g, diameter = 196.53–259.13 nm, and average size = 213.27 nm), whereas these microparticles were transformed to nanoscaled HgS particles (HgS NPs; BET surface area = 14.380 m 2 /g, diameter = 58.87–90.56 nm, and average size = 72.78 nm) by the action of ultrasonication. The as‐prepared HgS, HgS NPs in particular, afforded remarkable microbicidal activity against eight strains of filamentous and unicellular human pathogenic fungi and yeasts in comparison with cycloheximide. Remarkably, Aspergillus terreus grew up to 34.7 ± 1.88 mm in the absence of any fungicide, but HgS μPs, HgS NPs, and cycloheximide limited the fungal growth to 26 ± 0.94, 12.33 ± 1.6, and 28.3 ± 1.7 mm after incubation for 6 days. Besides, inhibition of Rhodotorula glutinis was of 7.6 ± 0.01 × 10 7 CFU/ml in control sample, but experiments included HgS μPs, HgS NPs, and cycloheximide limited the colony‐forming units of R. glutinis to 4.2 ± 0.01 × 10 7, 3.5 ± 0.02 × 10 7, and 5.9 ± 0.05 × 10 7 CFU/ml. Abstract : A mercuric salicylaldimine complex was introduced and analyzed by single‐crystal X‐ray diffraction (XRD). When the complex was reacted with thioacetamide under hydrothermal conditions, microscaled HgS particles (HgS μPs) were produced, and the microscaled HgS particles were downsized by ultrasonication to produce nanoscaled HgS particles (HgS μPs). The as‐formed HgS particles, particularly the nanoscaled ones, displayed remarkable microbicidal activity against eight strains of filamentous and unicellular human pathogenic fungi and yeasts. … (more)
- Is Part Of:
- Applied organometallic chemistry. Volume 35:Number 3(2021)
- Journal:
- Applied organometallic chemistry
- Issue:
- Volume 35:Number 3(2021)
- Issue Display:
- Volume 35, Issue 3 (2021)
- Year:
- 2021
- Volume:
- 35
- Issue:
- 3
- Issue Sort Value:
- 2021-0035-0003-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-12-16
- Subjects:
- crystallography -- fungi -- mercuric sulfide -- microparticles -- nanoparticles
Organometallic chemistry -- Periodicals
Organometallic compounds -- Periodicals
547.05 - Journal URLs:
- http://www3.interscience.wiley.com/cgi-bin/jhome/109566206 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/2676 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/aoc.6134 ↗
- Languages:
- English
- ISSNs:
- 0268-2605
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1576.270000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15754.xml