# Receptor-Mediated and Hydrolytic Denitrosylation of Dinitrosyl Iron Complexes to Yield Amorphous Fe x O y  and Its Photoinduced Transformation into Crystalline Fe@Fe x O y  Nanoparticles

**Authors:** Wun-Yan Wu, Yu-Shen Lin, Linda Iffland, Ulf-Peter Apfel, Tsai-Te Lu, Wen-Feng Liaw

PMC · DOI: 10.1021/acs.inorgchem.5c01434 · 2025-06-17

## TL;DR

This study shows how dinitrosyl iron complexes can be transformed into amorphous and then crystalline iron oxide nanoparticles through chemical and light-induced processes.

## Contribution

The paper introduces a novel dual mechanism for denitrosylation and the photoinduced transformation of iron complexes into structured nanoparticles.

## Key findings

- Denitrosylation of amp-DNIC occurs via receptor-mediated transfer and hydrolysis, releasing ·NO, N2O, and nitrite.
- Hydrolysis of amp-DNIC produces amorphous Fe x O y particles (amp-1) which transform into crystalline Fe@Fe x O y nanoparticles (amp-2) under light.
- Characterization techniques confirmed the structural and compositional changes during the transformation process.

## Abstract

In this study, denitrosylation of amine-bound {Fe­(NO)2}10 [(2-A)­Fe­(NO)2] (amp-DNIC)
was explored to occur through (a) receptor-mediated transfer of ·NO/[NO]− to [Mn­(TPP)­(Cl)] and (b) a hydrolytic process leading
to the liberation of ·NO together with N2O. In the
presence of the bifunctional ·NO/[NO]−-receptor
[Mn­(TPP)­(Cl)] (TPP = 5,10,15,20-tetraphenyl-21H,23H-porphine), amp-DNIC acts as a dual ·NO/[NO]− delivery reagent for the conversion of [Mn­(TPP)­(Cl)]
into [Mn­(TPP)­(NO)] and [Mn­(TPP)­(NO)2]. Alternatively, incubation
of amp-DNIC in an acetonitrile solution containing 5%
deaerated water resulted in its hydrolytic transformation into amorphous
Fe
x
O
y
 particles
(amp-1) accompanied by the release of ·NO (∼75%),
N2O (∼10%), and nitrite (∼6%). Upon irradiation
of amp-DNIC in the presence of the photosensitizer Eosin
Y and the sacrificial reductant TEA, the formation of cubic and crystalline
Fe@Fe
x
O
y
 core–shell
composite carbonaceous material (amp-2) was characterized
by high-resolution X-ray diffraction (HRXRD), field emission scanning
electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS),
X-ray absorption near-edge spectroscopy (XANES), and extended X-ray
absorption fine structure (EXAFS). Based on the mechanisms described
above, the hydrolytic transformation of amp-DNIC into amp-1 occurred, followed by the photoinduced structural rearrangement
of amp-1, amorphous Fe
x
O
y
 particles, into amp-2, the
cubic and crystalline Fe@Fe
x
O
y
 core–shell composite carbonaceous material.

## Linked entities

- **Chemicals:** Mn(TPP)(Cl) (PubChem CID 91864721), TPP (PubChem CID 164912), Eosin Y (PubChem CID 11048), NO (PubChem CID 24822), N2O (PubChem CID 948), nitrite (PubChem CID 946)

## Full-text entities

- **Chemicals:** Mn(TPP)(Cl)] (MESH:C101263), acetonitrile (MESH:C032159), water (MESH:D014867), O (MESH:D010100), nitrite (MESH:D009573), 5,10,15,20-tetraphenyl-21 (-), porphine (MESH:C107018), Eosin Y (MESH:D004801), N (MESH:D009584), [NO (MESH:D009614), Fe (MESH:D007501), H (MESH:D006859), amine (MESH:D000588)

## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12216227/full.md

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Source: https://tomesphere.com/paper/PMC12216227