tunable photoluminescence (PL), as well as cheap and readily available precursor sources. Consequently, CQDs now occupy many frontiers of nanotechnology. Nevertheless, several challenges that hinder their full exploitation still exist, for instance, there is minimum degree of control of optical properties and morphologies during their formation. Additionally, CQDs produced from mixtures of starting precursor materials pose impurity problems to their specific applications. Furthermore, aggregation induced PL quenching of CQDs has limited their highly desired applications in the solid state. This is because in colloidal state, nature of solvent media and PH easily influence optical properties of CQDs, [6] which is unwarranted for their function as bio/chemical sensors. Herein, we present facile synthesis of multifunctional CQDs by femtosecond laser ablation of single precursor molecules in solution with feasibility of in situ monitoring and their incorporation into mesoporous silica films for solid-state applications.Fast and easy preparation of CQDs with high purity and high fluorescence (FL) quantum yield (QY) is essential for their applications in bio/chemical sensing. In this article, emphasis is on versatile CQDs that are capable of sensing glucose molecules among other applications. Most glucose sensors are based on electrochemical technique [7] with recent studies emphasizing non-enzymatic electrochemical glucose sensing. [8][9][10] Detection of glucose from FL signal of CQDs is also an active area of research. [11,12] Because of its superior sensitivity, FLbased glucose sensing has great potential for ultimate design of non-invasive detection of glucose in biological fluids such as tears, sweat, and saliva where glucose concentration is about one order of magnitude lower than in blood. Non-invasive glucose sensing would be a boon to diabetic patients struggling with finger pricking method. Boronic acids are promising molecules for non-enzymatic FL detection of glucose because they form sensitive and specific reversible covalent complexes with 1,3 diols of glucose molecules. [13] To obtain boronic acid doped CQDs, we employed femtosecond (fs) pulsed laser ablation of 2-aminopyrimidine-5-boronic acid (2-APBA) in solution in a one step process without