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Organic Chemistry Lab
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An organic chemistry lab that synthesizes molecules whose emission color changes when rubbed, as well as chiral molecules.

AboutAbout the lab
Synthesizing new molecules and uncovering their functions.
The Organic Chemistry Lab uses synthetic organic chemistry to study photochemistry and supramolecular chemistry.
The lab designs and synthesizes organic molecules that do not exist in nature, and pursues the synthesis of molecules and the elucidation of their functions in parallel.
It focuses in particular on molecules with functions related to luminescence and chirality.
Lab visits by undergraduate students of the Department of Chemistry and Life Science are accepted at any time.
Key terms
- Mechanochromic luminescence
- A phenomenon in which the emission color of a solid reversibly changes when a mechanical stimulus such as rubbing is applied.
- Chiral molecule
- A molecule that cannot be superimposed on its mirror image, like the right and left hands. The right-handed and left-handed forms show different biological activities.
- Asymmetric synthesis
- A technique for selectively making either the right-handed or left-handed form of a chiral molecule. Ordinary organic synthesis produces both in a 1:1 ratio.
NewsLab news
A paper from the lab has been accepted by Crystal Growth & Design
A review article by Associate Professor Ito has been accepted by Bulletin of the Chemical Society of Japan
A co-authored paper with Kindai University has been published in Advanced Optical Materials
A co-authored paper with Kobe University has been accepted by Chemical Communications
Associate Professor Ito received the SHGSC Japan Award of Excellence 2026
ResearchResearch themes
Using the techniques of synthetic organic chemistry, it is possible to design and synthesize organic molecules that do not exist in nature. The lab synthesizes "original molecules" with new structures and studies their functions, particularly those related to luminescence and chirality.
*Illustrative imageMolecules whose emission color changes when rubbed
The lab aims to clarify which molecules show mechanochromic luminescence, in which the emission color of a solid changes reversibly under mechanical stimuli such as rubbing, and to realize this property as desired. It works on developing donor–acceptor molecules with new designs and on two-component systems combined with other luminescent molecules.
*Illustrative imageNew functions of chiral molecules
Using asymmetric synthesis techniques, the lab has established a method to obtain chiral diol molecules through "double asymmetric addition," which creates two stereocenters at once. With this method, it is developing chiral molecules with new functions, such as molecules whose circularly polarized luminescence can be switched.
MembersFaculty
- Associate ProfessorSuguru Ito
VoicesStudent voices
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Report an errorAbout the images
The top and research theme images are illustrative and were not taken at the lab. They are cropped from Wikimedia Commons images. Cropped CC BY-SA images are provided under the same CC BY-SA license as the original (version shown on each line).
- Top image: “Praseodymium chloride heptahydrate under fluorescent lamp light and halogen lamp light” Spidey71 / CC BY-SA 3.0 (cropped)
- Molecules whose emission color changes when rubbed: “Fluorescent pigment” FK1954 / Public domain (cropped)
- New functions of chiral molecules: “Mecoprop-racemic-dimer-from-xtal-labelled-3D-balls” Ben Mills / Public domain (cropped)
- Related lab (Aramaki Lab): “Dülmen, Dernekamp, Seifenblase” Dietmar Rabich / CC BY-SA 4.0 (cropped)
- Related lab (Polymer Chemistry Lab): “Epoxy-resin-used-for-bonding-of-FRP-sheets” Sherif El-Gamal, Khalifa Al-Jabri, Ahmed Al-Mahri, Saud Al-Mahrouqi / CC BY 4.0 (cropped)
- Related lab (Photofunctional Chemistry Lab): “Optical photochromic lenses” Albarubescens / CC BY-SA 4.0 (cropped)
- Related lab (Matsuzawa Lab): “Superheroes of our time” Gn.zhigerbayeva / CC BY-SA 4.0 (cropped)
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