Interplay between π-Conjugation and Exchange Magnetism in One- Dimensional Porphyrinoid Polymers
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15640%2F22%3A73627008" target="_blank" >RIV/61989592:15640/22:73627008 - isvavai.cz</a>
Alternative codes found
RIV/68378271:_____/22:00561260 RIV/61388955:_____/22:00561260
Result on the web
<a href="https://pubs.acs.org/doi/10.1021/jacs.2c02700" target="_blank" >https://pubs.acs.org/doi/10.1021/jacs.2c02700</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/jacs.2c02700" target="_blank" >10.1021/jacs.2c02700</a>
Alternative languages
Result language
angličtina
Original language name
Interplay between π-Conjugation and Exchange Magnetism in One- Dimensional Porphyrinoid Polymers
Original language description
The synthesis of novel polymeric materials with porphyrinoid compounds as key components of the repeating units attracts widespread interest from several scientific fields in view of their extraordinary variety of functional properties with potential applications in a wide range of highly significant technologies. The vast majority of such polymers present a closed-shell ground state, and, only recently, as the result of improved synthetic strategies, the engineering of open-shell porphyrinoid polymers with spin delocalization along the conjugation length has been achieved . Here, we present a combined strategy toward the fabrication of one-dimensional porphyrinoid-based polymers homocoupled via surface-catalyzed [3 + 3] cycloaromatization of isopropyl substituents on Au(111). Scanning tunneling microscopy and noncontact atomic force microscopy describe the thermal-activated intra-and intermolecula r oxidative ring closure reactions as well as the controlled tip-induced hydrogen dissociation from the porphyrinoid units. In addition, scanning tunneling spectroscopy measurements, complemented by computational investigations, reveal the open-shell character, that is, the antiferromagnetic singlet ground state (S = 0) of the formed polymers, characterized by singlet-triplet inelastic excitations observed between spins of adjacent porphyrinoid units. Our approach sheds light on the crucial relevance of the pi-conjugation in the correlations between spins, while expanding the on-surface synthesis toolbox and opening avenues toward the synthesis of innovative functional nanomaterials with prospects in carbon-based spintronics.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10301 - Atomic, molecular and chemical physics (physics of atoms and molecules including collision, interaction with radiation, magnetic resonances, Mössbauer effect)
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN
0002-7863
e-ISSN
1520-5126
Volume of the periodical
144
Issue of the periodical within the volume
28
Country of publishing house
US - UNITED STATES
Number of pages
7
Pages from-to
"12725 "- 12731
UT code for WoS article
000829574800001
EID of the result in the Scopus database
2-s2.0-85134720574