![创建参考文献 1 (a)、1 (b)，而不是 [1]、[2] 等](https://linux22.com/image/460291/%E5%88%9B%E5%BB%BA%E5%8F%82%E8%80%83%E6%96%87%E7%8C%AE%201%20(a)%E3%80%811%20(b)%EF%BC%8C%E8%80%8C%E4%B8%8D%E6%98%AF%20%5B1%5D%E3%80%81%5B2%5D%20%E7%AD%89.png)
我希望创建一个参考文献列表，其中我可以选择将参考文献编号为 1 (a)、1(b) 等，而不是 [1]、[2] 等。理想情况下，我希望将参考文献 6 和 7 标记为 6 (a)、6 (b)，其余标记为 1、2 等。
有什么办法可以做到这一点吗？我是 Tex 的初学者，所以请忽略我的一些愚蠢错误。以下是我使用的 MWE 和 7 个参考资料。很抱歉 MWE 太长了，我使用的是大学模板。
非常感谢您的帮助和时间。
尼拉詹
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%---------------------------------------------------
%AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
%---------------------------------------------------
\title{\textbf{Title}
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\begin{document}
%-------To do------------
% Ctrl r: Schrodinger Schr\"{o}dinger
%------------------------
\setlength{\droptitle}{-80pt}
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\vspace{-8ex}
\section{Background}
\label{s:bckg}
I have one reference here.\cite{Das2017} I have two more references here.\cite{savoie2015,kordnezhadian2022}
My third reference is here.\cite{kordnezhadian2022}
Fourth\cite{matsumoto2018} and 5th reference.\cite{rueping2017}
\section{Aims and Objectives}
\label{s:a_o}
No reference in this section
\section{Scientific Approach/Methodology}
\label{s:methods}
Two references here.\cite{Mayr2008,mayrdatabase}
\section{Resources}
\label{s:resources}
No refs here.
\bibliography{sf5}
\bibliographystyle{rsc}
\end{document}
Bibliography files
@article{Kordnezhadian2022,
author = {Reza Kordnezhadian and Bing‐Yu Li and Armir Zogu and Joachim Demaerel and Wim M. De Borggraeve and Ermal Ismalaj},
doi = {10.1002/chem.202201491},
file = {::},
issn = {0947-6539},
journal = {Chem. – A Eur. J.},
month = {oct},
number = {60},
title = {{Chemistry of Pentafluorosulfanyl Derivatives and Related Analogs: From Synthesis to Applications}},
url = {https://onlinelibrary.wiley.com/doi/10.1002/chem.202201491},
volume = {28},
year = {2022},
pages = {1-26}
}
@article{Savoie2015,
author = {Paul R. Savoie and John T. Welch},
doi = {10.1021/cr500336u},
file = {::},
issn = {0009-2665},
journal = {Chem. Rev.},
month = {jan},
number = {2},
pages = {1130--1190},
title = {{Preparation and Utility of Organic Pentafluorosulfanyl-Containing Compounds}},
url = {https://pubs.acs.org/doi/10.1021/cr500336u},
volume = {115},
year = {2015}
}
@article{Rueping2017,
abstract = {A protocol for the fast and selective two-electron reduction of the potent greenhouse gas sulfur hexafluoride (\ce{SF6}) by organic electron donors at ambient temperature has been developed.},
author = {Magnus Rueping and Pavlo Nikolaienko and Yury Lebedev and Alina Adams},
doi = {10.1039/C7GC00877E},
file = {::},
issn = {1463-9262},
journal = {Green Chem.},
number = {11},
pages = {2571--2575},
title = {{Metal-free reduction of the greenhouse gas sulfur hexafluoride, formation of \ce{SF5}-containing ion pairs and the application in fluorinations}},
url = {http://xlink.rsc.org/?DOI=C7GC00877E},
volume = {19},
year = {2017}
}
@article{Das2017,
author = {Prajwalita Das and Etsuko Tokunaga and Norio Shibata},
journal = {Tetrahedron Lett.},
title = {Tetrahedron Letters Recent advancements in the synthesis of pentafluorosulfanyl (SF 5 )-containing heteroaromatic compounds},
url = {https://doi.org/10.1016/j.tetlet.2017.11.015},
year = {2017},
pages = {4803},
volume = {58}
}
@article{Matsumoto2018,
author = {Kazuhiko Matsumoto and Yuki Haruki and Shunsuke Sawada and Shigeyuki Yamada and Tsutomu Konno and Rika Hagiwara},
doi = {10.1021/acs.inorgchem.8b02655},
issn = {0020-1669},
issue = {23},
journal = {Inorg. Chem.},
month = {12},
pages = {14882-14889},
title = {Stabilization of SF 5 – with Glyme-Coordinated Alkali Metal Cations},
volume = {57},
url = {https://pubs.acs.org/doi/10.1021/acs.inorgchem.8b02655},
year = {2018},
}
@article{Mayr2008,
abstract = {Comprehensive nucleophilicity scales including π-, n- and σ-nucleophiles have been constructed using benzhydrylium ions and structurally related quinone methides as reference electrophiles. It is shown how the correlation (Eqn (1)) log k20°C = s(E + N), where s and N are nucleophile-specific parameters and E is an electrophile-specific parameter, has recently been employed to characterize further classes of nucleophiles (phosphines, amines, isonitriles, trifluoro-methanesulfonyl- substituted carbanions) and electrophiles (2-benzylideneindan-1,3-diones and benzylidenebarbituric acids). Practical applications of the reactivity parameters E, N and s for developing Friedel-Crafts alkylations in neutral alcoholic or aqueous solution and for characterizing nucleophilic organocatalysts will be discussed. Eventually, a new correlation equation will be presented, which includes Eqn (1), the Ritchie equation (nucleophilic additions to stabilized carbocations), and the Swain-Scott equation (nucleophilic substitutions of methyl halides) as special cases. Copyright © 2008 John Wiley & Sons, Ltd.},
author = {Herbert Mayr and Armin R. Ofial.},
doi = {10.1002/poc.1325},
issn = {08943230},
issue = {7-8},
journal = {J. Phys. Org. Chem.},
keywords = {Electrophilicity,Intrinsic barriers,Kinetics,Linear free energy relationships,Nucleophilicity,Organocatalysis},
month = {7},
pages = {584-595},
title = {Do general nucleophilicity scales exist?},
volume = {21},
year = {2008},
}
@misc{mayrdatabase,
title = { Mayr's Database of Reactivity Parameters},
url = {https://www.cup.lmu.de/oc/mayr/reaktionsdatenbank/},
journal = {Database of Nucleophilicities and Electrophilicities},
note = {accessed on 24/01/2023},
urldate = {24/01/2023}
}