Speaker: Dr. Akshay Nair
Marie Curie Fellow, (CIQUS), Spain
Title: "Photocatalytic Valorization of Methane and Other
Gaseous Alkanes" and "Post-doctoral funding
opportunities: Career growth".
Day and Date: Friday, November 21, 2025
Time: 16.00 Hrs.
Venue: Room no. 350, Chemistry Department
Second floor, Annex
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Hosted by Prof. Chandra M. R. Volla
Abstract Methane and other gaseous (C2-C4) alkanes are one of the
most abundant carbon-based feedstocks on this planet. They
are typically burned off as fuel or used for steam cracking.
These processes are energy-intensive and contribute to the
release of greenhouse gases. As a result, it’s highly
important to develop protocols that allow efficient chemical
transformation of these feedstocks. Although rewarding
from a sustainability and efficiency standpoint, the
functionalization of gaseous alkanes remains challenging
due to their extreme inertness. The C–H bonds in gaseous
alkanes have high bond dissociation energy (99–105 kcal
mol− 1
) and ionization potential (∼12.5 eV), along with low acidity (pKa ∼50–51). Also, their gaseous nature
and low solubility in common organic solvents add further complications. As a result, only a few reports exist
documenting their efficient functionalization. In particular, highly versatile transformations such as crosscouplings, asymmetric catalysis, cascade cyclizations etc., remain unreported with methane and other gaseous
alkanes.
In this regard, we disclosed an arylative cross-coupling of gaseous alkanes with a range of aryl bromides.
1 The
reaction involves photocatalytic generation of alkyl radicals from gaseous alkanes and the subsequent nickelmediated cross-coupling of these radicals with aryl bromides. Next, we expanded this strategy for acylative
cross-coupling of gaseous alkanes.2 This protocol provides an efficient gateway for the upscaling of gaseous
alkanes to high-volume commodity ketones. Following this, we have developed the first cascade cyclization
of methane and gaseous alkanes.3 This transformation provides a gateway for rapidly achieving molecular
complexity using these simple alkanes. Very recently, we have unlocked the very first asymmetric
transformation of C2-C4 alkanes to carry out 1,2-dicarbofunctionalization of olefins.4 All these protocols
showcase excellent functional group tolerance while proceeding under mild energy-efficient conditions. These
methods offer promising avenues for the valorization of feedstock gaseous alkanes.