Related Experiment Video
Updated: Jan 9, 2026

Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations
Published on: October 12, 2019
Correlating Nanomechanical Behavior and Adsorption Performance in a Serendipitously Assembled Two-Dimensional
Ashis Chhetri1,2,3, Shamim Ahmad4, Sumana Podder1,2
1Inorganic Materials & Catalysis Division, CSIR-Central Salt & Marine Chemicals Research Institute, Bhavnagar 364002 Gujarat, India.
Abstract:
Hydrogen-bonded organic systems (HBOS) combine facile synthesis, solution processability, regenerability, and water stability, making them attractive for the design of functional materials. Motivated by the limited report on chiral HBOS, we explored the hydrothermal assembly of melamine (M) and l-glutamic acid (L-GA) and unexpectedly yielded a crystalline 2D melamine-cyanuric acid (M-CA) adduct. In this transformation, L-GA served both as an acid catalyst promoting partial in situ hydrolysis of M to cyanuric acid (CA), and as a structure-directing agent, facilitating the M-CA self-assembly. Nanoindentation revealed that M-CA exhibits significantly higher penetration depths than those of M and CA, consistent with its layered packing and presence of hollow hexagonal channels. In contrast, M displayed the highest elastic modulus and hardness due to its rigid herringbone packing. Energy framework analysis linked the nanomechanical behavior of the crystals to the differences in hydrogen-bonding strength and topology. Functionally, M-CA demonstrated superior guest adsorption (rhodamine B 96.75 mg g-1 and methyl orange 102.50 mg g-1) with excellent recyclability over multiple cycles, outperforming both M and CA by ∼4-fold. These results establish a correlation between the structure of HBOS, nanomechanical properties, and adsorption performance, offering insights into the design of hydrogen-bonded functional materials.
Related Concept Videos
Noncovalent Attractions in Biomolecules
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
Hydrogen Bonds
Molecular Orbital Theory II
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
MO Theory and Covalent Bonding
¹H NMR: Long-Range Coupling
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene...

