From ligand exchange to reaction intermediates: what does really happen during the synthesis of emissive complexes?‡

Literature Information

Publication Date 2017-12-20
DOI 10.1039/C7CP07142F
Impact Factor 3.676
Authors

P. Polzin, I. V. Eliani, J. Ströh, M. Braun, N. Ruser, P. Rönfeldt, F. Bertram, C. Näther, S. Wöhlbrandt, M. Suta, H. Terraschke


View Original

Abstract

In situ monitoring of the formation of emissive complexes is essential to enable the development of rational synthesis protocols, to provide accurate control over the generation of structure-related properties (such as luminescence) and to facilitate the development of new compounds. In situ luminescence analysis of coordination sensors (ILACS) utilizes the sensitivity of the spectroscopic properties of lanthanide ions to their coordination environment to detect structural changes during crystallization processes. Here, ILACS was utilized to monitor the formation of [Eu(bipy)2(NO3)3] (bipy = 2,2′-bipyridine) during co-precipitation synthesis. Validity of the ILACS results was ensured by concomitant utilization of in situ monitoring of other reaction parameters, including in situ measurements of pH value, ionic conductivity, and infrared spectra, as well as ex situ and synchrotron-based in situ X-ray diffraction analyses. Gradual desolvation of the Eu3+ ions and attachment of ligands were detected by an exponential increase of the intensity of the 5D0 → 7FJ (J = 0–4) transitions in the emission spectrum. Additionally, the in situ emission spectra show a decrease in the crystallization rate and an increase in the induction time in response to a reduction in the concentration of the starting solutions from 12 mM until crystallization ceased at starting reactant concentrations <6 mM. An increase to a three-fold higher concentration leads to the formation of a reaction intermediate, and its stability was determined to be highly concentration-dependent. The in situ luminescence measurements also demonstrated the existence of a ligand exchange process within the [Eu(bipy)2(NO3)3] complex upon addition of a phen (phen = 1,10′-phenanthroline) solution and the generation of a new phen-containing emissive complex. In attempting to solve the structure of this new phen-containing complex, a different, but nevertheless previously unsynthesized complex, [Eu(phen)2(NO3)3]bipy, was obtained, which shows characteristic Eu3+ luminescence in the red spectral range.

Related Literature

The molecular structure of the surface of water–ethanol mixtures

Johannes Kirschner, Anderson H. A. Gomes, Olle Björneholm, Vincenzo Carravetta, Niklas Ottosson, Arnaldo Naves de Brito, Huib J. Bakker

2021-05-11 Paper

DOI: 10.1039/D0CP06387H

Anomalous patterns of Saffman–Taylor fingering instability during a metastable phase separation

Ryuta X. Suzuki, Hikari Tada, Sae Hirano, Takahiko Ban, Manoranjan Mishra, Risa Takeda, Yuichiro Nagatsu

2021-04-15 Paper

DOI: 10.1039/D0CP05810F

Identification and electronic characterization of four cyclodehydrogenation products of H2TPP molecules on Au(111)

Jianchen Lu, Binbin Da, Wei Xiong, Renjun Du, Zhenliang Hao, Zilin Ruan, Yong Zhang, Shijie Sun, Lei Gao, Jinming Cai

2021-04-22 Paper

DOI: 10.1039/D1CP01040A

A kinetic model of thin-film fluorescent sensors for strategies to enhance chemical selectivity

Iain A. Campbell, Graham A. Turnbull

2021-04-29 Paper

DOI: 10.1039/D1CP00835H

Bond-forming and electron-transfer reactivity between Ar2+ and N2

Sam Armenta Butt, Stephen D. Price

2021-04-26 Paper

DOI: 10.1039/D1CP00918D

Encapsulating aluminum nanoparticles into carbon nanotubes for combustion: a molecular dynamics study

Liang Song, Feng-Qi Zhao, Si-Yu Xu, Xue-Hai Ju

2021-04-22 Paper

DOI: 10.1039/D1CP01135A

Deactivation-free ethanol steam reforming at nickel-tipped carbon filaments

Yutichai Mueanngern, Cheng-Han Li, Meiling Spelic, Joshua Graham, Nathan Pimental, Yehia Khalifa, Joerg R. Jinschek, L. Robert Baker

2021-05-04 Paper

DOI: 10.1039/D1CP00637A

Contrasting the EXAFS obtained under air and H2 environments to reveal details of the surface structure of Pt–Sn nanoparticles

Haoliang Huang, Verónica Celorrio, Diego Gianolio, Christopher Hardacre, Dan J. L. Brett, Andrea E. Russell

2021-05-11 Paper

DOI: 10.1039/D1CP00979F

You might also like

Compound Q&A

How should waste containing N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide (CAS: 898825-89-3) be handled?

Waste containing N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide (CAS: 898825-89-3...

898825-89-3N-Methoxy-N-methyl-1...
Compound Q&A

How should N-(4-Biphenylyl)dibenzo[b,d]furan-4-amine (CAS: 1318338-47-4) be stored?

N-(4-Biphenylyl)dibenzo[b,d]furan-4-amine should be stored in a tightly sealed c...

1318338-47-4N-(4-Biphenylyl)dibe...
Compound Q&A

What is the market or research trend for 3-Acetamido-5-amino-2,4,6-triiodobenzoic acid (CAS: 1713-07-1)?

The market for 3-Acetamido-5-amino-2,4,6-triiodobenzoic acid (CAS: 1713-07-1) is...

1713-07-13-Acetamido-5-amino-...
Compound Q&A

How should Benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-beta-D-galactopyranoside (CAS: 61820-03-9) be stored?

Benzyl 2-O-acetyl-3,4,6-tri-O-benzyl-beta-D-galactopyranoside (CAS: 61820-03-9) ...

61820-03-9Benzyl 2-O-acetyl-3,...
Compound Q&A

What regulatory guidelines apply to 2-Ethylpiperazine dihydrochloride (CAS: 438050-52-3)?

2-Ethylpiperazine dihydrochloride (CAS: 438050-52-3) is regulated under the Glob...

438050-52-32-Ethylpiperazine di...
Compound Q&A

What regulatory guidelines apply to 1,1'-[1,3-Phenylenebis(methylene)]bis(3-methyl-1H-pyrrole-2,5-dione) (CAS: 119462-56-5)?

1,1'-[1,3-Phenylenebis(methylene)]bis(3-methyl-1H-pyrrole-2,5-dione) (CAS: 11946...

119462-56-51,1'-[1,3-Phenyleneb...
Compound Q&A

Are there alternatives to 5-Fluoro-2-(1-pyrrolidinyl)pyridine (CAS: 1287217-79-1) in synthesis?

Several alternatives can be used in the synthesis of 5-Fluoro-2-(1-pyrrolidinyl)...

1287217-79-15-Fluoro-2-(1-pyrrol...
Compound Q&A

What precautions should be taken when handling 6-Bromoimidazo[1,2-a]pyridin-8-amine (CAS: 676371-00-9)?

When handling 6-Bromoimidazo[1,2-a]pyridin-8-amine, it is important to wear appr...

676371-00-96-Bromoimidazo[1,2-a...
Compound Q&A

Are there alternatives to (2S,4R)-4-(4-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride (CAS: 1049740-22-8) in synthesis?

Alternatives to (2S,4R)-4-(4-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochlo...

1049740-22-8(2S,4R)-4-(4-Nitrobe...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.