\documentclass[journal=jacsat,manuscript=article]{achemso}
\usepackage{graphicx}
\usepackage{amsmath,amssymb}
\usepackage{chemformula}
\usepackage{booktabs}
\author{First A.~Author}
\affiliation[University X]{Department of Chemistry, University X, City, Country}
\author{Second B.~Author}
\altaffiliation{Present address: Institute Y.}
\affiliation[University X]{Department of Chemistry, University X, City, Country}
\author{Third C.~Author}
\email{[email protected]}
\affiliation[Institute Y]{Institute Y, City, Country}
\title[Short title]{Full Title of an ACS Article}
\keywords{chemistry, synthesis, catalysis, characterization}
\begin{document}
\begin{abstract}
Abstracts are up to 250 words. State the problem, approach, and findings.
\end{abstract}
\section{Introduction}
Motivate the chemical problem, review prior art~\cite{ref1}.
\section{Experimental Section}
\subsection{Materials}
All chemicals were obtained from commercial sources.
\subsection{Synthesis}
Reaction of \ch{Pd(OAc)2} with ligand L in toluene at 80\,$^\circ$C gave the complex.
\begin{equation*}
\ch{Pd(OAc)2 + 2 L -> Pd(L)2(OAc)2}
\end{equation*}
\section{Results and Discussion}
X-ray crystallography confirmed the structure. Catalytic activity was
benchmarked against standard substrates.
\begin{table}
\centering
\caption{Catalytic yields.}
\begin{tabular}{lcc}
\toprule
Substrate & Yield (\%) & TON \\
\midrule
A & 92 & 1840 \\
B & 85 & 1700 \\
C & 78 & 1560 \\
\bottomrule
\end{tabular}
\end{table}
\section{Conclusions}
Summary.
\begin{acknowledgement}
We thank the NSF for funding.
\end{acknowledgement}
\begin{suppinfo}
Additional NMR spectra, crystallographic data (CIF).
\end{suppinfo}
\begin{thebibliography}{1}
\bibitem{ref1}
Author, A.; Author, B. Title. \emph{J. Am. Chem. Soc.} \textbf{2024}, \emph{146}, 1000--1010.
\end{thebibliography}
\end{document}

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