» Articles » PMID: 27382167

Polymorphism and Electronic Structure of Polyimine and Its Potential Significance for Prebiotic Chemistry on Titan

Overview
Specialty Science
Date 2016 Jul 7
PMID 27382167
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The chemistry of hydrogen cyanide (HCN) is believed to be central to the origin of life question. Contradictions between Cassini-Huygens mission measurements of the atmosphere and the surface of Saturn's moon Titan suggest that HCN-based polymers may have formed on the surface from products of atmospheric chemistry. This makes Titan a valuable "natural laboratory" for exploring potential nonterrestrial forms of prebiotic chemistry. We have used theoretical calculations to investigate the chain conformations of polyimine (pI), a polymer identified as one major component of polymerized HCN in laboratory experiments. Thanks to its flexible backbone, the polymer can exist in several different polymorphs, which are relatively close in energy. The electronic and structural variability among them is extraordinary. The band gap changes over a 3-eV range when moving from a planar sheet-like structure to increasingly coiled conformations. The primary photon absorption is predicted to occur in a window of relative transparency in Titan's atmosphere, indicating that pI could be photochemically active and drive chemistry on the surface. The thermodynamics for adding and removing HCN from pI under Titan conditions suggests that such dynamics is plausible, provided that catalysis or photochemistry is available to sufficiently lower reaction barriers. We speculate that the directionality of pI's intermolecular and intramolecular =N-H(…)N hydrogen bonds may drive the formation of partially ordered structures, some of which may synergize with photon absorption and act catalytically. Future detailed studies on proposed mechanisms and the solubility and density of the polymers will aid in the design of future missions to Titan.

Citing Articles

The Composition and Chemistry of Titan's Atmosphere.

Nixon C ACS Earth Space Chem. 2024; 8(3):406-456.

PMID: 38533193 PMC: 10961852. DOI: 10.1021/acsearthspacechem.2c00041.


Crossroads at the Origin of Prebiotic Chemical Complexity: Hydrogen Cyanide Product Diversification.

Sandstrom H, Rahm M J Phys Chem A. 2023; 127(20):4503-4510.

PMID: 37166122 PMC: 10226121. DOI: 10.1021/acs.jpca.3c01504.


Multivariate Analysis Applied to Microwave-Driven Cyanide Polymerization: A Statistical View of a Complex System.

Perez-Fernandez C, Gonzalez-Toril E, Mateo-Marti E, Ruiz-Bermejo M Polymers (Basel). 2023; 15(2).

PMID: 36679288 PMC: 9866860. DOI: 10.3390/polym15020410.


Semiconducting Soft Submicron Particles from the Microwave-Driven Polymerization of Diaminomaleonitrile.

Ruiz-Bermejo M, Garcia-Armada P, Valles P, de la Fuente J Polymers (Basel). 2022; 14(17).

PMID: 36080535 PMC: 9460857. DOI: 10.3390/polym14173460.


An XPS study of HCN-derived films on pyrite surfaces: a prebiotic chemistry standpoint towards the development of protective coatings.

Perez-Fernandez C, Ruiz-Bermejo M, Galvez-Martinez S, Mateo-Marti E RSC Adv. 2022; 11(33):20109-20117.

PMID: 35479901 PMC: 9033743. DOI: 10.1039/d1ra02658e.


References
1.
Ruiz-Bermejo M, Zorzano M, Osuna-Esteban S . Simple Organics and Biomonomers Identified in HCN Polymers: An Overview. Life (Basel). 2014; 3(3):421-48. PMC: 4187177. DOI: 10.3390/life3030421. View

2.
R Schreiner P, Reisenauer H, Ley D, Gerbig D, Wu C, Allen W . Methylhydroxycarbene: tunneling control of a chemical reaction. Science. 2011; 332(6035):1300-3. DOI: 10.1126/science.1203761. View

3.
Goumans T, Kastner J . Hydrogen-atom tunneling could contribute to H2 formation in space. Angew Chem Int Ed Engl. 2010; 49(40):7350-2. DOI: 10.1002/anie.201001311. View

4.
Tomasko M, Archinal B, Becker T, Bezard B, Bushroe M, Combes M . Rain, winds and haze during the Huygens probe's descent to Titan's surface. Nature. 2005; 438(7069):765-78. DOI: 10.1038/nature04126. View

5.
Linder M, Brinck T . Synergistic activation of the Diels-Alder reaction by an organic catalyst and substituents: a computational study. Org Biomol Chem. 2009; 7(7):1304-11. DOI: 10.1039/b818655c. View