Related Experiment Video
Updated: Feb 7, 2026

Pairwise Growth Competition Assay for Determining the Replication Fitness of Human Immunodeficiency Viruses
Published on: May 4, 2015
Heterogeneous Parahydrogen Pairwise Addition to Cyclopropane
Oleg G Salnikov1,2, Kirill V Kovtunov1,2, Panayiotis Nikolaou3
1International Tomography Center, SB RAS, 3 A Institutskaya st., Novosibirsk, 630090, Russia.
Researchers developed a new method for hyperpolarized propane production using cyclopropane and parahydrogen. This advance enables enhanced pulmonary MRI imaging with conventional scanners, offering a non-toxic contrast agent.
Area of Science:
- Medical Imaging
- Nuclear Magnetic Resonance (NMR) Spectroscopy
- Catalysis
Background:
- Hyperpolarized gases significantly advance functional pulmonary imaging.
- Hyperpolarized propane is an emerging, non-toxic contrast agent for pulmonary MRI.
- Proton-hyperpolarized propane is compatible with conventional MRI scanners.
Purpose of the Study:
- To demonstrate the feasibility of propane hyperpolarization via hydrogenation of cyclopropane with parahydrogen.
- To achieve high levels of NMR-visible hyperpolarized propane for enhanced MRI.
Main Methods:
- Utilized heterogeneous Rh/TiO2 hydrogenation catalyst.
- Employed 82% parahydrogen enrichment for propane synthesis.
- Investigated propane hyperpolarization through cyclopropane hydrogenation.
Main Results:
- Achieved 1H propane polarization up to 2.4%, exceeding levels from propylene precursor.
- Demonstrated NMR-visible hyperpolarized propane via a reaction pathway involving C-H bond cleavage.
- Sufficient NMR signal enhancement for 2D gradient echo MRI of a 5.5 mL phantom at 1x1 mm2 resolution.
Conclusions:
- Propane hyperpolarization via cyclopropane hydrogenation is feasible and efficient.
- This method yields higher polarization levels compared to using propylene.
- The resulting hyperpolarized propane is suitable for high-resolution pulmonary MRI applications.
Related Concept Videos
Conjugate Addition (1,4-Addition) vs Direct Addition (1,2-Addition)
Conjugate addition results in a thermodynamically stable product. The reaction retains the stronger C=O bond at the expense of the weaker C=C π bond. The process is slow as the β carbon is less electrophilic than the carbonyl carbon.
Direct addition products are...
Conjugate Addition of Enolates: Michael Addition
Vector Addition of Forces
To understand the concept of vector addition, consider the scenario of a ship being pulled by two small tugboats. The two forces, F1 and F2, act concurrently on the ship in different directions. The parallelogram law can be used to calculate the net force...
Additional Subnuclear Structures
The nucleus contains many membrane-less subnuclear organelles or nuclear bodies, such as nucleoli, Cajal bodies, speckles,...
Additional Subnuclear Structures
Radical Formation: Addition
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an...

