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A review on recent advances of iron-based macrocyclic complexes as prominent candidate for several potential applications

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Abstract

The scope of possible applications such as catalysis, bioinorganic, medical region, coordination chemistry, bio-mimetic, etc., is the main driving force for the expansion of macrocyclic and supramolecular chemistry as the demand for novel and superior complexes increased day by day for evident advanced applications. Herein this review article, we tried to succinct the chemistry of iron-based macrocyclic complexes published during the 2015–2023 period with their potent applications. Macrocycles with benign presence of first-row transition metals have gained more focus because of gigantic potent biological applications, namely, antimicrobial, anti-biofilm, anti-inflammatory, antibacterial, antifungal, antiviral, anti-carcinogenic, antifertility, antioxidant, magnetic resonance imaging contrast agents, anti-HIV activities, and many more. Broadly, these biological activities are influenced by metal ion’s chemical properties such as chelation, solubility, dipole moment, and conductivity and by the formation of their macrocyclic compounds. Iron-based macrocycles are involved in various biological functions such as metabolism, respiration, DNA synthesis, catalytic oxidation, etc., which are a few of them, so in this concise review, we presented the recent advancement of iron-based macrocycles complexes in a summarized systematic way, with synthetic routes, structural elucidation, catalytic performance, and their role as biologically active core for copious activities. We hope that it will be fruitful for young researchers working in this field.

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Abbreviations

Al:

Aluminum

AIDS:

Acquired immune deficiency syndrome

A. niger :

Aspergillus niger

A. alternata :

Alternaria alternata

B. cereus :

Bacillus cereus

BM:

Bohr magneton

B. subtilis :

Bacillus subtilis

B. stearothermophilus :

Bacillus stearothermophilus

[Bu4N] [BF4]:

Tetrabutylammonium tetrafluoroborate

Ca:

Calcium

CAs:

Contrast agents

C. albican :

Candida albican

CH3OH:

Methanol

Co:

Cobalt

Cr:

Chromium

Cu:

Copper

CV:

Cyclic voltammetry

DAT:

Diaminotoluene

DBM:

Dibenzoyl methane

DMF:

Dimethylfuran

DMSO:

Dimethyl sulfoxide

DNA:

Deoxyribonucleic acid

DTA:

Differential thermal analysis

E. coli :

Escherichia coli

ESI–MS:

Electrospray ionization–mass spectrometry

ESR:

Electron spin resonance

EWG:

Electron-withdrawing group

Fe:

Iron

F. oxysporum :

Fusarium oxysporum

FT-IR:

Fourier transform infrared spectroscopy

GBCA:

Gadolinium-based contrast agent

Gd:

Gadolinium

GDD:

Gadolinium deposition disease

GPX4:

Glutathione peroxidase

HIV:

Human immunodeficiency virus

HPLC:

High-performance liquid chromatography

H2Q:

Hydroquinone

IBCA:

Iron-based contrast agents

L. infantum :

Leishmania infantum

MIC:

Minimal inhibitory concentration

Mg:

Magnesium

MMCs:

Metal macrocyclic complexes

Mn:

Manganese

Mo:

Molybdenum

MRI:

Magnetic resonance imaging

MSN:

Macromolecular, supramolecular, and nanochemistry

Ni:

Nickel

NMR:

Nuclear magnetic resonance

NPs:

Nanoparticles

NrF2 :

Nuclear factor erythriod-2-related factor 2

OEP:

Octaethyl porphyrin

ORR:

Oxygen reduction reaction

P. aeruginosa :

Pseudomonas aeruginosa

P. funiculosum :

Penicillium funiculosum

P. putida :

Pseudomonas putida

PH :

Potential of hydrogen

PTT:

Polytrimethylene terephthalate

ROS:

Reactive oxygen species

S. aureus :

Staphylococcus aureus

S. cerevisiae :

Saccharomyces cerevisiae

S. griseus :

Streptomyces griseus

S. typhi :

Salmonella typhi

SDA:

Sabouraud dextrose agar

TACN:

Triazacyclononane

t-CDTA:

Trans-cyclohexane diamine tetra-acetic acid

TEAP:

Tetra-ethyl-ammonium-perchlorate

TGA:

Thermogravimetric analysis

TMB:

3,3,5,5-Teramethyl benzidine

T. reesei :

Trichoderma reesei

UV:

Ultraviolet

XAS:

X-ray absorption spectroscopy

XPS:

X-ray photoelectron spectroscopy

Zn:

Zinc

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Acknowledgements

Authors are thankful to the Department of Chemistry, University of Rajasthan, Jaipur (India), for providing all kinds of facilities and support related to this work.

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Authors and Affiliations

  1. Department of Chemistry, University of Rajasthan, Jaipur, 302004, India

    Om Prakash Gurjar, Pooja Saini, Sushama Kumari, Krishna Atal & Swati Bugalia

  2. Department of Chemistry, Government Lohia College, Churu, 331001, India

    Urmila Phageria

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  3. Sushama Kumari
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  4. Krishna Atal
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All authors contributed a lot for preparing the manuscript entitled “A review on recent advances of iron-based macrocyclic complexes as prominent candidate for several potential applications.” For this, literature survey was carried out by SB, OPG, PS, KA, and SK, research scholars of University of Rajasthan, Jaipur (INDIA). All authors read and approved the final manuscript.

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Correspondence to Swati Bugalia.

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Gurjar, O.P., Saini, P., Kumari, S. et al. A review on recent advances of iron-based macrocyclic complexes as prominent candidate for several potential applications. J IRAN CHEM SOC 21, 305–326 (2024). https://doi.org/10.1007/s13738-023-02934-3

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